Class I
Ongoing
Reported Aug 19, 2026
Kian Pee Wan Capsules, 30-count bottles
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Product was sold to individual consumers via ebay third party seller.
- Firm
- Buy-Herbal
- Recall began
- Mar 21, 2026
- Quantity
- 71 bottles
- Codes
- All lots within expiry.
- FDA IDs
- D-0769-2026 / event 98650
Class I
Ongoing
Reported Aug 19, 2026
Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VM...
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
USA Nationwide
- Firm
- Victory Medical Center Pharmacy
- Recall began
- Jul 1, 2026
- Quantity
- 91
- Codes
- Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
- FDA IDs
- D-0772-2026 / event 99509
Class I
Ongoing
Reported Aug 19, 2026
Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution, Manufactured by: Liebel-Flarshei...
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
Distributed Nationwide in the US and Mexico.
- Firm
- Liebel-Flarsheim Company LLC
- Recall began
- Jul 31, 2026
- Quantity
- 3,486 500mL-vials
- Codes
- Lot # 25ZF3670, Exp Date: May 31, 2027.
- FDA IDs
- D-0773-2026 / event 99510
Class II
Ongoing
Reported Aug 19, 2026
SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Ino...
CGMP Deviations:Noted during FDA inspection
Distributed Nationwide in the USA
- Firm
- Shoolin Pharma Chem LLP
- Recall began
- Aug 3, 2026
- Quantity
- 25KG, 250-1gm bags
- Codes
- Batch SDC2505001, Date of Expiry: April 30, 2030.
- FDA IDs
- D-0759-2026 / event 99547
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65...
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Nationwide within the U.S
- Firm
- Apollo Care, LLC
- Recall began
- Jul 29, 2026
- Quantity
- 250 vials.
- Codes
- Lot: AC-017273, Exp. 12/12/2026.
- FDA IDs
- D-0755-2026 / event 99505
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Nationwide within the U.S
- Firm
- Apollo Care, LLC
- Recall began
- Jul 29, 2026
- Quantity
- 56,918 vials.
- Codes
- Lot: AC-017108, Exp. 11/17/2026; AC-017110, Exp. 11/20/2026; AC-017112, Exp. 11/21/2026; AC-017142, AC-017144, Exp. 12/10/2026; AC-017166, AC-017167, AC-017177, AC-017213, AC-01722...
- FDA IDs
- D-0747-2026 / event 99505
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Nationwide within the U.S
- Firm
- Apollo Care, LLC
- Recall began
- Jul 29, 2026
- Quantity
- 23,029 vials.
- Codes
- Lot: AC-017114, Exp. 11/24/2026; AC-017164, AC-017204, AC-017205, Exp. 12/31/2026.
- FDA IDs
- D-0748-2026 / event 99505
Class II
Ongoing
Reported Aug 19, 2026
CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-603-51
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
Nationwide within the U.S
- Firm
- Heritage Pharmaceuticals Inc
- Recall began
- Jul 30, 2026
- Quantity
- Not specified
- Codes
- Lot #: 2411550, Exp. 2026/NOV.
- FDA IDs
- D-0768-2026 / event 99526
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65...
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Nationwide within the U.S
- Firm
- Apollo Care, LLC
- Recall began
- Jul 29, 2026
- Quantity
- 250 vials.
- Codes
- Lot: AC-017271, Exp. 12/12/2026.
- FDA IDs
- D-0753-2026 / event 99505
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Nationwide within the U.S
- Firm
- Apollo Care, LLC
- Recall began
- Jul 29, 2026
- Quantity
- 37,546 vials.
- Codes
- Lot: C-017115, Exp. 11/25/2026; AC-017163, Exp. 12/31/2026; AC-017169, AC-017170, AC-017171, Exp. 12/31/2026; AC-017230, AC-017231, Exp. 5/5/2027.
- FDA IDs
- D-0749-2026 / event 99505
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Nationwide within the U.S
- Firm
- Apollo Care, LLC
- Recall began
- Jul 29, 2026
- Quantity
- 4,748 vials.
- Codes
- Lot: AC-017131, Exp. 8/30/2026.
- FDA IDs
- D-0752-2026 / event 99505
Class II
Ongoing
Reported Aug 19, 2026
CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC...
Lack of assurance of sterility. The recall is due to potential contamination
Nationwide in the USA.
- Firm
- Prestige Brands Holdings
- Recall began
- Jul 29, 2026
- Quantity
- 39,060 15mL-bottles
- Codes
- Lot 2552A, Exp 09/30/2027
- FDA IDs
- D-0766-2026 / event 99532