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Browse Drug Recalls

1,788 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 1,788 FDA drug recall enforcement actions. Each entry includes the product description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Drug Safety Recalls

Browse 1,788 FDA drug recalls in 2019.

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DateProductReasonClassFirm
Oct 15, 2019 Viatrexx-MuSkel-Neural, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio ... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Facial, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorpo... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Ithurts, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorp... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Immunexx, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incor... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Arthros, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorp... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Mesenchyme, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Inc... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Infla, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorpor... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-GI, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporate... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Prolo, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorpor... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Neuro 3, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorp... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorp... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Lymph 1, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorp... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Collagen, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incor... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Connectissue, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio I... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Ouch, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorpora... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Articula, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incor... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Inc... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 15, 2019 Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorpora... Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its steri... Class II 8046255 Canada Inc. DBA Viatrexx
Oct 11, 2019 Levetiracetam Injection, 500 mg/5mL, 10 single-use 5 mL vials, Rx only, Manuf... Labeling: Incorrect or Missing Package Insert - the incorrect package insert version was attached. Class III X-Gen Pharmaceuticals Inc.
Oct 10, 2019 Lyophilized Human Chorionic Gonadotropin 5,000 USP Units For injection, Rx On... Lack of Sterility Assurance. Class II Innoveix Pharmaceuticals Inc
Oct 10, 2019 Lyophilized Chorionic Gonadotropin 11,000 USP Units for Injection, Rx Only, ... Lack of Sterility Assurance. Class II Innoveix Pharmaceuticals Inc
Oct 10, 2019 Lyophilized Sermorelin w/ GHRP2 3 mg For injection, Rx Only, Compounded by: I... Lack of Sterility Assurance. Class II Innoveix Pharmaceuticals Inc
Oct 10, 2019 Lyophilized Human Chorionic Gonadotropin 5,500 USP Units For injection, Rx On... Lack of Sterility Assurance. Class II Innoveix Pharmaceuticals Inc
Oct 9, 2019 PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Sodium Chloride ... GMP Deviations: potential glass contamination Class II Nephron Pharmaceuticals Corporation dba Nephron...
Oct 9, 2019 del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephr... Lack of Assurance of Sterility; bags have potential to leak Class II Nephron Pharmaceuticals Corporation dba Nephron...
Oct 9, 2019 PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Sodium Chlo... GMP Deviations: potential glass contamination Class II Nephron Pharmaceuticals Corporation dba Nephron...
Oct 9, 2019 PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Sodium Chlorid... GMP Deviations: potential glass contamination Class II Nephron Pharmaceuticals Corporation dba Nephron...
Oct 9, 2019 Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl; 25 g L-Lysi... Lack of Assurance of Sterility; bags have potential to leak Class II Nephron Pharmaceuticals Corporation dba Nephron...
Oct 9, 2019 Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose ... Crystallization: Presence of particulate matter identified as API crystallization Class II Ingenus Pharmaceuticals Llc
Oct 7, 2019 Rifampin for Injection, USP, 600 mg/vial, Rx only, Manufactured for: Mylan I... Failed Impurities/Degradation Specifications: discoloration due to elevated unknown impurity resu... Class II Mylan Laboratories Limited (Sterile Products Di...
Oct 4, 2019 Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar... Presence of Foreign Substance; Fiber particles. Class III KVK-Tech, Inc.
Oct 2, 2019 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 ... Lack of Assurance of Sterility: Bag has the potential to leak. Class II Pfizer Inc.
Oct 1, 2019 Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injectio... Lack of sterility assurance. Class II New Vitalis Pharmacy LLC dba New Vitalis Pharmacy
Oct 1, 2019 Ranitidine Tablets, USP 75 mg, a.) 30 count bottles (NDC 69842-871-30) b.) 80... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 71713-203-02), b.)9... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Dr. Reddy's Ranitidine Capsules, USP 300 mg, a.) 30 count bottles (NDC 55111-... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 0363-0010-34), b.) ... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Dr. Reddy's Ranitidine Tablets, USP 75 mg, 60 count bottles, NDC 55111-131-60... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Dr. Reddy's Ranitidine Tablets, USP 150 mg, 24 count bottles, NDC 55111-404-3... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Dr. Reddy's: Ranitidine Capsules 150 mg, Rx a.) 60 count bottles (NDC 55111-... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 150 mg, a.) 95 count bottles (NDC 43598-808-62), b.) ... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Zentrip (meclizine Hydrochloride), 25 mg strips, 8-strips per box, Distribute... Subpotent Drug Class III Sato Pharmaceutical Inc.
Oct 1, 2019 Ranitidine Tablets, USP 150 mg, 190 count bottles (2x95) Tray (Sam's Club) OT... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 30142-505-34), b.) ... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 150 mg, NDC 57896-717 (GeriCare) OTC CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 75 mg, a.) 30- count bottles (NDC 0363-0131-30), b.) ... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 WAL-DRAM 2 (meclizine Hydrochloride) 25 mg tablets, packaged in a) 12 count (... Subpotent Drug Class III Sato Pharmaceutical Inc.
Oct 1, 2019 Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 63868-480-24), b.) ... CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 75 mg, NDC 57896-715 (GeriCare) OTC. CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.
Oct 1, 2019 Ranitidine Tablets, USP 75 mg 30 count bottles (NDC 30142-131-30) (Kroger) CGMP Deviations: Presence of NDMA impurity detected in product. Class II Dr. Reddy's Laboratories, Inc.

Frequently Asked Questions

When a drug safety issue is identified — through FDA inspections, laboratory testing, adverse event reports, or manufacturer quality checks — the responsible company issues a recall to remove the affected products from the market. Pharmacies pull the product from shelves, and consumers are advised to contact their healthcare provider for alternatives.

The leading causes include cGMP deviations, impurity contamination (including nitrosamines like NDMA), failed dissolution or stability testing, sterility issues, potency problems, labeling errors, and foreign particle contamination.

Use the search and filter tools on this page to look up specific medications, active ingredients, or manufacturers. Each recall entry includes the product description, lot numbers, and distribution details.