Ongoing FDA Recalls

A no-JavaScript view of ongoing recalls in the latest Recall Radar snapshot. Ongoing status means the FDA record has not been marked completed or terminated in the loaded enforcement data. For a compact overview, use the snapshot summary, and check source status for openFDA refresh evidence. Use the private match checker, product clue index, code clue index, or reason clue index to compare product, firm, code, and FDA problem clues against the loaded snapshot. For the freshest report date, use newly reported recalls, or browse by FDA report date. For highest-risk, broad-distribution, or location-clue records, use highest concern recalls, nationwide recalls, or location clues. For next steps after a possible match, use the recall action checklist, and use the recall field guide to interpret record fields. For all loaded records, use the latest recall digest or interactive Recall Radar.

GeneratedSep 23, 2026, 8:30 PM EDT
Ongoing Loaded36
Class I Ongoing6
Food / Drugs / Devices12 / 12 / 12
Drugs Not Yet Classified Ongoing Reported Sep 16, 2026

fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City Lake, Fayetteville, AR, NDC 73013-1013-01.

Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026).

Nationwide within the U.S

Firm
OurPharma LLC
Recall began
Sep 3, 2026
Quantity
1,610 bags
Codes
Lot #: 101301260605, BUD: 12/9/2026.
FDA IDs
Not specified / event 99837
Source
openFDA source record
Drugs Class III Ongoing Reported Sep 16, 2026

Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-255-01.

Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent.

Nationwide within the U.S

Firm
Ajanta Pharma USA Inc
Recall began
Aug 25, 2026
Quantity
403,200 tablets
Codes
Lot #: DJ23254, Exp. Date 11/30/2026; DJ10205, Exp. Date 04/30/2027.
FDA IDs
D-0836-2026 / event 99733
Source
openFDA source record
Drugs Class III Ongoing Reported Sep 16, 2026

Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 078...

Subpotent Drug

USA Nationwide

Firm
ImprimisRx NJ LLC
Recall began
Aug 24, 2026
Quantity
772 bottles
Codes
Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
FDA IDs
D-0835-2026 / event 99756
Source
openFDA source record
Food Class I Ongoing Reported Sep 16, 2026

Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506

Potential E. coli and Salmonella contamination

Wholesale consignees in 16 states: CA, FL, HI, IL, MA, MN, MO, MT, NY, OH, OR, PA, TN, SC, TX, UT; Puerto Rico; Canada, Mexico, Tahiti, and Venezuela

Firm
International Sprout Holdings, Inc
Recall began
Aug 23, 2026
Quantity
43,799 lbs.
Codes
ISS Lot # SAL2-24JB
FDA IDs
H-1341-2026 / event 99822
Source
openFDA source record
Drugs Class I Ongoing Reported Sep 16, 2026

Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06

Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.

U.S. Nationwide.

Firm
Baxter Healthcare Corporation
Recall began
Aug 17, 2026
Quantity
606 bags
Codes
Lot #: Y495066, Exp. Date July 31, 2027
FDA IDs
D-0850-2026 / event 99679
Source
openFDA source record
Food Class II Ongoing Reported Sep 16, 2026

Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz

Undeclared milk and pecans

IA, IL, IN, OH

Firm
Ferrero USA
Recall began
Aug 14, 2026
Quantity
1488 retail units
Codes
All best by codes that were sold 8/7/2026 to 8/14/2026
FDA IDs
H-1334-2026 / event 99682
Source
openFDA source record
Food Class I Ongoing Reported Sep 16, 2026

Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower, net wt. 3oz (85g). UPC 6 28634 44216 6. Ingredients: Broccoli, Cauliflower, Tapioca Flour, Coconut Oil, Salt, Whit...

Undeclared Wheat.

Product was sold in the U.S.

Firm
EXOTIQUE FOODS CANADA
Recall began
Aug 7, 2026
Quantity
68 cases
Codes
Best Before: 2026 AUGUST 31
FDA IDs
H-1330-2026 / event 99636
Source
openFDA source record
Food Class II Ongoing Reported Sep 16, 2026

Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold screw on closure. UPC: 50040360530

Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.

Product is sold exclusively from the recalling firm's online website nationwide.

Firm
L-Nutra Inc
Recall began
Aug 7, 2026
Quantity
8,529 jars
Codes
Lot code: L2755 Expiration: 02 Jan 2027
FDA IDs
H-1335-2026 / event 99675
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR(8028), 4. 32FR(8032), 5. 36FR(8036);

An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

US Nationwide distribution.

Firm
Atrium Medical Corporation
Recall began
Aug 7, 2026
Quantity
3618
Codes
1. Model Number(Size): 8016(16FR); UDI-DI: 00650862130164; Lot Number: ME244878; 2. Model Number(Size): 8024(24FR); UDI-DI: 00650862130249; Lot Number: ME244835; 3. Model Number(Si...
FDA IDs
Z-3111-2026 / event 99680
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028), 2. 36FR(15036);

An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

US Nationwide distribution.

Firm
Atrium Medical Corporation
Recall began
Aug 7, 2026
Quantity
256
Codes
1. Model Number(Size): 15028(28FR); UDI-DI: 00650862150285; Lot Number: ME244891; 3. Model Number(Size): 15036(36FR); UDI-DI: 00650862150360; Lot Number: ME244850;
FDA IDs
Z-3113-2026 / event 99680
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at wavelengths of 532 nm and 1064 nm through a fiber-optic han...

Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.

Worldwide distribution - US Nationwide and the countries of Canada and European Union.

Firm
Lutronic Corporation
Recall began
Aug 6, 2026
Quantity
1065
Codes
Lot Code: Model: DermaV Software Version: 1.06 UDI #: 08800291820200 Serial Numbers: DV025A010, DV025A011, DV025A012, DV025A013, DV025A014, DV025A015 DV025A016, DV025A018, DV025A01...
FDA IDs
Z-3110-2026 / event 99601
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201

Hemodialysis concentrates contain high endotoxin levels

Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.

Firm
Nipro Renal Soultions USA, Corporation
Recall began
Aug 5, 2026
Quantity
3,286 cases
Codes
BC-100 - Lot:N4L022 (exp.11/13/2026), N4L037(exp.11/18/2026) BC+201- Lot: N4L010(exp.11/06/2026)
FDA IDs
Z-3133-2026 / event 99573
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))

Hemodialysis concentrates contain high endotoxin levels

Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.

Firm
Nipro Renal Soultions USA, Corporation
Recall began
Aug 5, 2026
Quantity
2,327 cases
Codes
DB+201-2.1: Lot -NDB5E004(exp.4/30/2027) DB+201-25: Lots - NDB5M011(Exp.12/05/2027, NDB4J003(exp.9/25/2026)
FDA IDs
Z-3134-2026 / event 99573
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)

Hemodialysis concentrates contain high endotoxin levels

Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.

Firm
Nipro Renal Soultions USA, Corporation
Recall began
Aug 5, 2026
Quantity
100 drums/1072 cases
Codes
LC+200-D: Lot-N4J030 (Exp.9/20/2026), N5D043(Exp.4/16/2027); LC+225: Lot-N6A025(Exp.1/8/2028)
FDA IDs
Z-3136-2026 / event 99573
Source
openFDA source record
Food Class I Ongoing Reported Sep 16, 2026

Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen

The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

The adulterated product was distributed to the following states: VA, NY, NJ, MI

Firm
EURO FOODS GROUP USA NJ INC
Recall began
Aug 1, 2026
Quantity
53 boxes
Codes
BATCH NO: 130 EF, 146 EF SERIAL NUMBER: 5055192640140 PRODUCT CODE: 28DSUM
FDA IDs
H-1331-2026 / event 99684
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B

The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation.

US Nationwide distribution in the states of CA, GA, WA.

Firm
Windstone Medical Packaging, Inc.
Recall began
Jul 29, 2026
Quantity
3,260 kits
Codes
UDI-DI:B098AMS12394B0; Lot Numbers: 241907, 241223, 241034, 240904, 240705, 240633, 240269, 238361, 238197, 238146, 238085, 238084, 238041, 237957, 237901, 237843, 237663, 237444,...
FDA IDs
Z-3138-2026 / event 99658
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US...

Due to a damaged (over stretched) membrane tail that causes an intermittent fault.

Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME MI, MN, NC, NJ, NM, NV, NY, OH, OK, OR, PA, SD,TN, TX, UT, VA, WA, WI, WV and WY. The countries of Argentina, Australia,...

Firm
HeartSine Technologies Ltd
Recall began
Jul 27, 2026
Quantity
11,912
Codes
350P US Device, US English - 2 Min CPR Item code: 350-STR-US-10 UDI-DI codes: 0506016712067 Serial Numbers: 22D91164357L22 22D91164989L22 22D91180808K23 23D98000415K23 23D98000597K...
FDA IDs
Z-3120-2026 / event 99568
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801¿ 10801741024808 00801741024818¿ 10801741024815 00...

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...

Firm
C.R. Bard Inc
Recall began
Jun 25, 2026
Quantity
12,463 trays/kits
Codes
Catalog Numbers / UDI codes: 899914 / 00801741024801¿ 10801741024808 Lot Number: NGKU4611 899916 / 00801741024818¿ 10801741024815 Lot Numbers: NGKU2448 NGKU4610 899918 / 0080174102...
FDA IDs
Z-3114-2026 / event 98840
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 947316 947318 UDI codes: 00801741024924¿ 10801741024921 008017410...

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...

Firm
C.R. Bard Inc
Recall began
Jun 25, 2026
Quantity
283883 trays/kits
Codes
Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter Catalog Numbers / UDI codes: 947314 / 00801741024924¿ 10801741024921 Lot Numbers: NGKT2599 NGKU0115 947316 / 0080174102...
FDA IDs
Z-3115-2026 / event 98840
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 10801741121064 SureStep" Foley Tray System Complet...

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...

Firm
C.R. Bard Inc
Recall began
Jun 25, 2026
Quantity
33850 units/kits
Codes
SureStep" Foley Tray System Add-A-Foley Catheter A153200 / 00801741121067¿ 10801741121064 Lot Number: NGKS2397 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter A3044...
FDA IDs
Z-3118-2026 / event 98840
Source
openFDA source record
Devices Class II Ongoing Reported Sep 16, 2026

Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 00801741143243 SureStep" Foley Tray System...

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...

Firm
C.R. Bard Inc
Recall began
Jun 25, 2026
Quantity
364
Codes
(Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 00801741143243 Lot Number: NGKT2492 SureStep" Foley Tray System Bardex¿ IC Complete...
FDA IDs
Z-3119-2026 / event 98840
Source
openFDA source record
Drugs Class III Ongoing Reported Sep 9, 2026

Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus P...

Failed dissolution specifications.

US Nationwide.

Firm
Supernus Pharmaceuticals, Inc.
Recall began
Aug 31, 2026
Quantity
11304 bottles
Codes
Lot# 2145283, Exp Date: 31-Mar-2030.
FDA IDs
D-0833-2026 / event 99767
Source
openFDA source record
Drugs Class II Ongoing Reported Sep 9, 2026

traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o, Zagreb, Croatia, Manufactured For: Teva Pharmaceuticals, Parsip...

Presence of Foreign Tablets/Capsules

U.S. Nationwide

Firm
Teva Pharmaceuticals USA, Inc
Recall began
Aug 24, 2026
Quantity
175,392 bottles
Codes
Lot: 1394026, Exp. 02/2028.
FDA IDs
D-0834-2026 / event 99734
Source
openFDA source record
Drugs Class III Ongoing Reported Sep 9, 2026

Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC#: 60687-481-21, (Individual...

Labeling: Label Mix-up

US Nationwide.

Firm
American Health Packaging
Recall began
Aug 19, 2026
Quantity
10,953 cartons.
Codes
Lot # 1030023, Exp Date: 06/30/2027.
FDA IDs
D-0840-2026 / event 99674
Source
openFDA source record
Food Class III Ongoing Reported Sep 9, 2026

Prince ITALIAN BREAD; Sesame; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FLOUR, NIACIN, FERROUS SULFATE, THIAMIN MONONITRATE, RIBOFLAVI...

Sesame is not declared in the ingredient statement but is declared in the statement of identity.

New York.

Firm
Prince Bakery Inc
Recall began
Aug 13, 2026
Quantity
150 units (total)
Codes
No codes
FDA IDs
H-1304-2026 / event 99646
Source
openFDA source record
Food Class III Ongoing Reported Sep 9, 2026

Prince ITALIAN BREAD; Sesame; ITALIAN & FRENCH BREAD, LARGE; NET WEIGHT 12 OZ. (340g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FLOUR< NIACIN, FERROUS SULFATE...

Sesame is not declared in the ingredient statement but is declared in the statement of identity.

New York.

Firm
Prince Bakery Inc
Recall began
Aug 13, 2026
Quantity
150 units (total)
Codes
No codes
FDA IDs
H-1305-2026 / event 99646
Source
openFDA source record
Drugs Class II Ongoing Reported Sep 9, 2026

Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL Single-Dose Container, Rx only, Sterile, Baxter Healthcare Corporation, Deerfield, IL, 600...

CGMP Deviations

US Nationwide; Puerto Rico; and Chile.

Firm
Baxter Healthcare Corporation
Recall began
Aug 6, 2026
Quantity
N/A
Codes
Lot # NC193672, NC193795, Exp Date: 04/30/2028; Lot # NC194198, Exp Date: 05/31/2028.
FDA IDs
D-0811-2026 / event 99500
Source
openFDA source record
Drugs Class II Ongoing Reported Sep 9, 2026

CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/mL) in GALAXY Single-Dose Container, Manufactured and Marketed by: Baxter Healthc...

CGMP Deviations

US Nationwide; Puerto Rico; and Chile.

Firm
Baxter Healthcare Corporation
Recall began
Aug 6, 2026
Quantity
N/A
Codes
Lot # NC177818, Exp Date: 12/31/2026; Lot # NC188869, Exp Date: 12/31/2027.
FDA IDs
D-0813-2026 / event 99500
Source
openFDA source record
Drugs Class II Ongoing Reported Sep 9, 2026

Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield...

CGMP Deviations

US Nationwide; Puerto Rico; and Chile.

Firm
Baxter Healthcare Corporation
Recall began
Aug 6, 2026
Quantity
N/A
Codes
Lot # NC185424, Exp Date: 2/12/2027; Lot # NC185479, Exp Date: 2/13/2027; Lot # NC193948, Exp Date: 10/23/2027.
FDA IDs
D-0815-2026 / event 99500
Source
openFDA source record
Drugs Class II Ongoing Reported Sep 9, 2026

Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Co...

CGMP Deviations

US Nationwide; Puerto Rico; and Chile.

Firm
Baxter Healthcare Corporation
Recall began
Aug 6, 2026
Quantity
N/A
Codes
Lot # NC193856, Exp Date: 04/18/2028.
FDA IDs
D-0821-2026 / event 99500
Source
openFDA source record
Food Class II Ongoing Reported Sep 9, 2026

Weis (Fresh From the Orchard ) Pasteurized Apple Cider, Contains 100 % Juice, the product comes in the following sizes: Pints, 1/2 Gallon, Gallon, plastic jug. 6 1/2 - gallon jugs...

Product has high patulin levels

The recalled product was distributed to the State of PA.

Firm
WEIS MARKETS, INC.
Recall began
Aug 6, 2026
Quantity
Pints : 360 , 1/2 Gallon : 855, Gallon - 765
Codes
pull date/expiration date, etc. 7/17/26, 8/4/26, 8/13/26, 8/28/26, 9/4/26, 9/11/26, 9/30/26
FDA IDs
H-1308-2026 / event 99638
Source
openFDA source record
Drugs Class I Ongoing Reported Sep 9, 2026

Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only,...

Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

USA Nationwide.

Firm
OPTIMAL BALANCE PHARMACY
Recall began
Aug 5, 2026
Quantity
53 vials
Codes
Lot#: LG342009076, Beyond Use Date: 10/4/26
FDA IDs
D-0851-2026 / event 99662
Source
openFDA source record
Food Class II Ongoing Reported Sep 9, 2026

Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop's Homestyle Foods, LLC Richmond, VA 23230

Foreign object: metal fragments

Product was shipped to the following states: KY, NC, VA & WVA.

Firm
Ukrop's Homestyle Foods LLC
Recall began
Jul 30, 2026
Quantity
150/4lb units
Codes
Best By 07/06/26 to Best By 08/03/26
FDA IDs
H-1327-2026 / event 99548
Source
openFDA source record
Food Class III Ongoing Reported Sep 9, 2026

Wonton Specialist Inc. Pan Fried Noodle, 16 oz and 5lb packaged in clear plastic bags

Undeclared FD&C Red No. 40

NY, NJ, PA

Firm
Wonton Specialists
Recall began
Jul 28, 2026
Quantity
500 bags
Codes
No codes.
FDA IDs
H-1320-2026 / event 99508
Source
openFDA source record
Food Class III Ongoing Reported Sep 9, 2026

Wonton Specialist Inc. Cooked Noodle, 16 oz and 5 lb - packaged in clear plastic bags

Undeclared FD&C Red No. 40

NY, NJ, PA

Firm
Wonton Specialists
Recall began
Jul 28, 2026
Quantity
700 bags
Codes
No codes.
FDA IDs
H-1325-2026 / event 99508
Source
openFDA source record
Food Class I Ongoing Reported Sep 9, 2026

OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags. INGREDIENTS: Processed Dehydrated Yam Flour, freshness preserved by...

Undeclared milk.

Domestic: CA, GA, IL, NJ, NY, TX Foreign: Canada, Australia

Firm
Fayus Inc.
Recall began
Jul 6, 2026
Quantity
Unknown
Codes
All batch codes.
FDA IDs
H-1329-2026 / event 99368
Source
openFDA source record