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  1. FDA Recalls
  2. ›Drug Recalls

FDA Drug Recalls

Recalls of prescription drugs, over-the-counter medications, and compounded pharmaceuticals.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 4961–4980 of 17,755 recalls

Class IIITerminated

Asenapine Sublingual Tablets, 5 mg, Rx Only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020 NDC 42794-016-10.

SigmaPharm Laboratories LLC

Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent

April 19, 2021 · DrugView details →
Class IIITerminated

Asenapine Sublingual Tablets, 10 mg, Rx only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020, NDC 42794-017-10

SigmaPharm Laboratories LLC

Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent

April 19, 2021 · DrugView details →
Class IITerminated

Estradiol Transdermal System Delivers 0.0375 mg/day, 8 Systems/box, Rx only, Mfd. by: Noven Pharmaceuticals, Inc. Miami, Florida 33186 Dist. by: Noven Therapeutics, LLC Miami, Florida 33186, NDC 68968-3437-8

Noven Pharmaceuticals Inc

Defective Delivery System: Out of specification for release rate testing and shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience patches that do not stick well to the skin.

April 16, 2021 · DrugView details →
Class IITerminated

Minivelle (estradiol transdermal system) Delivers 0.075 mg/day, 8 patches/box, Rx only, Mfd. by: Noven Pharmaceuticals, Inc. Miami, Florida 33186 Dist. by: Noven Therapeutics, LLC Miami, Florida 33186, NDC 68968-6675-8

Noven Pharmaceuticals Inc

Defective Delivery System: Out of specification for release rate testing and shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience patches that do not stick well to the skin.

April 16, 2021 · DrugView details →
Class IITerminated

Oxygen, Compressed, USP UN 1072, packaged in cylinders labeled as: a) M6 Medical Gas Cylinder, b) C Medical Gas Cylinder; c) D Medical Gas Cylinder; d) E Medical Gas Cylinder; e) M Medical Gas Cylinder; f) H Medical Gas Cylinder, Rx only, Grace Healthcare 1418 31st Avenue Gulfport, MS 39501 228-863-3331

Grace Healthcare Medical, Inc

cGMP deviations

April 15, 2021 · DrugView details →
Class IITerminated

Delflex Peritoneal Dialysis Solution with 1.5% Dextrose, LM/LC, packaged in a case containing 2 x 6 Liter bags, Rx only, NDC 49230-206-60, Fresenius Medical Care North America, Waltham, MA 02451

Fresenius Medical Care, North America

Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.

April 14, 2021 · DrugView details →
Class IIITerminated

Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of 2 Strips Each), Manufactured by: Nomax, Inc, St. Louis, MO 63123, NDC: 51801-008-15

Nomax Inc

Subpotent Drug

April 13, 2021 · DrugView details →
Class IIOngoing

Cephalexin for Oral Suspension, Generic for Keflex, USP, Powder for Oral Suspension, 250 mg/5mL, Pkg Size 100, Rx only, Repackaged by Preferred Pharmaceuticals, Inc., Mfg: Ascend Laboratories, LLC, NDC #: 68788-7529-1,

Preferred Pharmaceuticals, Inc.

Failed Impurities/degradation specifications: Repackager recall due to Out of Specification detected by manufacturer for Individual Unidentified Impurity found during related substance test analysis of Cephalexin

April 12, 2021 · DrugView details →
Class IITerminated

Betadine (Povidone-Iodine) 5%, 0.5mL per syringe Single Use Syringe Rx only, For Topical Ophthalmic Use (DO NOT INJECT) STERILE OPHTHALMIC SOLUTION, PRESERVATIVE FREE, Edge Pharma, LLC 856 Hercules Dr. Colchester, VT 05446 Customer Service (USA) 1-802-992-1178

Edge Pharma, LLC

Defective container; syringe content migrating past the seal of the plunger may cause a lack of assurance of sterility

April 12, 2021 · DrugView details →
Class IIOngoing

Flurandrenolide Ointment USP, 0.05%, Net Wt. 60 grams, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310 NDC 52565-017-60

Teligent Pharma, Inc.

Failed Impurities/Degradation Specifications:

April 9, 2021 · DrugView details →
Class IOngoing

Ginseng Power 5000 capsule, 1- count per blister card, GS Natural Co, Los Angeles, CA 90010, UPC 0 40232 18144 3

NSNY Distributor Inc

Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/ or tadalafil

April 8, 2021 · DrugView details →
Class IOngoing

Premium OrgaZEN 7000 capsule, 1-count per blister card, distributed by: Nutra Vita Co, Santa Fe Springs, CA, Made in USA , UPC 0 40232 32555 7

NSNY Distributor Inc

Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/ or tadalafil

April 8, 2021 · DrugView details →
Class IIOngoing

PremierZen Black 5000, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ

Hyobin LLC

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil.

April 6, 2021 · DrugView details →
Class IIOngoing

Triple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ

Hyobin LLC

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil.

April 6, 2021 · DrugView details →
Class IIOngoing

PremierZen Extreme 3000, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ

Hyobin LLC

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil.

April 6, 2021 · DrugView details →
Class IITerminated

Itraconazole Capsules, 100 mg, 30-count bottles, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD 21801, NDC 59746-282-30.

Jubilant Cadista Pharmaceuticals, Inc.

Failed Dissolution Specifications

April 1, 2021 · DrugView details →
Class IIOngoing

IMPERIAL GOLD 2000, Male Sexual Performance Enhancement, 1 Capsule, UPC 718122040702

QMart

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

March 31, 2021 · DrugView details →
Class IITerminated

Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor, 16 fl. oz., 473 mL bottles Rx Only, Manufactured by: Mikart, LLC, Atlanta, GA 30318, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 10631-206-02.

SUN PHARMACEUTICAL INDUSTRIES INC

Microbial Contamination of Non-Sterile Product

March 31, 2021 · DrugView details →
Class IIOngoing

PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887

QMart

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

March 31, 2021 · DrugView details →
Class IIOngoing

Imperial Platinum 2000, 1 capsule, UPC 718122040702

QMart

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

March 31, 2021 · DrugView details →
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