FDA Enforcement Database

Drug Safety & Recalls Center

Access structured drug recall and safety information sourced directly from the U.S. Food & Drug Administration (FDA) OpenFDA Enforcement API. Stay informed on active market withdrawals, manufacturing defect notices, and drug safety advisories.

Last Synchronized
4 hours ago
Total FDA Recalls
1,244
Active / Ongoing
1,207
Critical (Class I)
66
Data Provenance & Source Transparency: All drug recall records displayed are retrieved directly from the official U.S. FDA OpenFDA Enforcement API. Questo organizes and presents this data for medical education and research without modifying original regulatory facts. Explore OpenFDA API Documentation →
Medical & Legal Disclaimer: The information on this page is compiled for informational and educational reference only and does not constitute medical advice or clinical diagnosis. Never discontinue, start, or substitute any medication without consulting your prescribing doctor or a licensed pharmacist. For urgent health concerns regarding a recalled product, contact your physician immediately or report adverse events to FDA MedWatch.
Showing 1–20 of 1,244 factual FDA recall reports
Class II (Moderate Risk)
Drug recall Recall #: D-0063-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Brush Buddies, Cookies 'n Cream Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-519-35, Item # 88519, UPC 8 10147 88519 0
Lots / Batch Codes & Expiration Dates
Lot# LWP250037221405, Exp Date: 07/04/2027; Lot# LWP250048151011, Exp Date: 11/11/2027; Lot# LWP250051162312A, Exp Date: 02/08/2028; Lot# LWP0054880903C, Exp Date: 04/30/2028.
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0065-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Brush Buddies, Whitening Anti-cavity Fluoride Toothpaste, with Baking Soda, (sodium monofluorophosphate 0.76%) Cool Mint, Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-007-07, ITEM # 999131, 8 50010 84249 3
Lots / Batch Codes & Expiration Dates
Lot # LWP250032331302B, Exp Date: 02/23/2027; Lot # LWP250034892603, Exp Date: 04/07/2027; Lot # LWP250032581702, Exp Date: 04/14/2027; Lot # LWP250045162409, Exp Date: 10/17/2027; Lot # LWP250032331302A, LWP250047640511A, Exp Date: 12/20/2027; Lot # LWP250051162312B, Exp Date: 01/04/2028; Lot # LWP0054880903B, Exp Date: 04/08/2028; Lot # LWP...
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0055-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Brush Buddies, Crayola, Silly Scents, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Bubble Gum Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-003-40, Item # 32731, UPC 8 50048 32731 3
Lots / Batch Codes & Expiration Dates
Lot # LWP240027561211, Exp Date: 12/07/2026; Lot # LWP250031970602, Exp Date: 02/28/2027; Lot # LWP250031980602, Exp Date: 03/11/2027; Lot # LWP250032381402, Exp Date: 03/17/2027; Lot # LWP250035680204, Exp Date: 04/30/2027; Lot # LWP250037682005A, Exp Date: 06/08/2027; Lot # LWP250048601811, Exp Date: 12/09/2027; Lot # LWP250051382412, Exp...
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0051-2027

LEVOXYL

Manufacturer / Recalling Firm: Pfizer
Reason for Recall: Subpotent Drug: confirmed out-of-specification (OOS) assay during stability testing.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg, 1000-count bottle, Rx only, Distributed by Pfizer Inc., New York, NY 10017, Made in Austria. NDC 60793-859-10
Lots / Batch Codes & Expiration Dates
Lot # 24W07, Exp: 11/30/2026
Distribution Scope
US Nationwide and Puerto Rico
Class II (Moderate Risk)
Drug recall Recall #: D-0070-2027

Testosterone Cypionate

Manufacturer / Recalling Firm: Right Value Drug Stores LLC
Reason for Recall: Lack of sterility assurance.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Testosterone Cypionate, 200 mg/mL, packaged in a) 5 mL vials (NDC 73271-1225-1) and b) 30 m vials ( NDC 73271-1226-2) This Is A Compounded Dug, Intramuscular Use, Office Use Only, 8400 Esters Blvd, STE 190, Irving, TX 75063.
Lots / Batch Codes & Expiration Dates
a) Lot 10212025@3, BUD 10/21/2026; 10292025@4, BUD 10/29/2026; 10282025@6, BUD: 10/29/2026; 12012025@1, BUD: 12/01/2026; 04072026@1, BUD: 04/01/2027; 05262026@3, BUD 05/08/2027; 05262026@7, BUD 11/17/2026; 05272026@1, BUD 05/08/2027; 05272026@2, BUD: 11/22/2026; 07032026@1, BUD 05/08/2027; 07022026@1, BUD: 05/08/2027; 07062026@3, BUD: 05/08/2027; 0...
Distribution Scope
Nationwide in the USA.
Class II (Moderate Risk)
Drug recall Recall #: D-0053-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Brush Buddies, Barbie, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Bubble Gum Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-001-40, Item# 88022, UPC 8 10147 88022 5
Lots / Batch Codes & Expiration Dates
Lot# LWP250031810502A, LWP250032571702A, Exp Date: 02/28/2027; Lot# LWP250035710304A, Exp Date: 04/27/2027; Lot # LWP250037812105, Exp Date: 06/03/2027; Lot # LWP250045750310, Exp Date: 02/19/2028; Lot # LWP260055421803, Exp Date: 05/13/2028.
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0061-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Brush Buddies, Vanilla Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-517-35, Item # 88517, UPC 8 10147 88517 6
Lots / Batch Codes & Expiration Dates
Lot# LWP250037221405, Exp Date: 07/04/2027; Lot# LWP250048151011, Exp Date: 11/11/2027; Lot# LWP250051162312A, Exp Date: 02/08/2028; Lot# LWP0054880903C, Exp Date: 04/30/2028.
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0069-2027

ARU

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
ARU, Toothpaste, Cavity Protection, 9 Ingredients, Cool Mint, (sodium fluoride 0.243%) Net Wt 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-785-35, Item # 88785, UPC 8 10147 88785
Lots / Batch Codes & Expiration Dates
Lot # LWP250047850611C, Exp Date: 12/22/2027; Lot # LWP260052612201C, Exp Date: 3/31/2028.
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0045-2027

AMLODIPINE AND OLMESARTAN MEDOXOMIL

Manufacturer / Recalling Firm: Ascend Laboratories, LLC
Reason for Recall: Out of specification due to dissolution.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Amlodipine and Olmesartan Medoxomil Tablets, 10mg/40mg, 30 Tablets, Rx only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-502-30.
Lots / Batch Codes & Expiration Dates
Lot # 25120696, Exp Date: December 31, 2026.
Distribution Scope
Nationwide within the United States
Class II (Moderate Risk)
Drug recall Recall #: D-0059-2027

evo

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
evo, Advanced Whitening, Anticavity Fluoride Toothpaste, (sodium fluoride 0.24%) Peppermint, Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-886-19, Item# 88619, UPC 8 10147 88619 7
Lots / Batch Codes & Expiration Dates
Lot# LWP250038750606, Exp Date: 08/03/2027; Lot# LWP250045152409A, Exp Date: 10/06/2027; Lot# LWP250046862110A, Exp Date: 11/11/2027; Lot# LWP250047640511B, Exp Date: 12/17/2027; Lot# LWP250051172312A, Exp Date: 01/25/2028; Lot# LWP250051182312B, Exp Date: 01/28/2028; Lot# LWP260052241401B, Exp Date: 03/18/2028; Lot# LWP0054880903F, Exp Date...
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0052-2027

LEVOXYL

Manufacturer / Recalling Firm: Pfizer
Reason for Recall: Subpotent Drug: confirmed out-of-specification (OOS) assay during stability testing.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg, 100 tablet bottle, Rx only, Distributed by Pfizer Inc., New York, NY 10017, Made in Austria. NDC 60793-859-01.
Lots / Batch Codes & Expiration Dates
Lot # 24W06, Exp: 11/30/2026
Distribution Scope
US Nationwide and Puerto Rico
Class II (Moderate Risk)
Drug recall Recall #: D-0064-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Brush Buddies, Chocolate Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-518-35, Item # 88518, UPC 8 10147 88518 3
Lots / Batch Codes & Expiration Dates
Lot# LWP250037221405, Exp Date: 07/04/2027; Lot# LWP250048151011, Exp Date: 11/11/2027; Lot# LWP250051162312A, Exp Date: 02/08/2028; Lot# LWP0054880903C, Exp Date: 04/30/2028.
Distribution Scope
US Nationwide.
Class I (High Risk)
Drug recall Recall #: D-0083-2027

ARGATROBAN

Manufacturer / Recalling Firm: Par Health USA, LLC
Reason for Recall: Particulate matter: particulate matter identified as cellulose, polystyrene, polyethylene teraphalate, stainless steel, or stopper material in the product solution.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Argatroban Injection, USP, 250 mg/2.5mL (100 mg/mL), 2.5 mL x 1 Single Dose Vial, Rx only, Manufactured for: Endo USA, Malvern,PA 19355/ Argatroban Injection, 250 mg/2.5mL (100 mg/mL), 2.5 mL x 1 Single Dose Vial, Rx only, Distributed by: Par Pharmaceutical, Cranbury, NJ 08512, NDC 42023-182-89.
Lots / Batch Codes & Expiration Dates
Lot #: 84193, Exp Date: 10/2026; 92880, Exp Date: 08/2027.
Distribution Scope
Nationwide within the United States
Class I (High Risk)
Drug recall Recall #: D-0084-2027

Glutathione Injection

Manufacturer / Recalling Firm: Greenwich Rx
Reason for Recall: Microbial Contamination of Sterile Products
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Glutathione Injection (Glutathione-L, Ascorbic Acid, Sodium Hydroxide, Bacteriostatic Water), 200 mg/mL, 10 mL multi-dose vial, Rx only, Subcutaneous Only, Greenwich Rx.
Lots / Batch Codes & Expiration Dates
Lot # 0060-062426-1, BUD: 10/02/2026; Lot # 0060-062726-1, BUD: 10/05/2026; Lot # 0060-070926-1, BUD: 10/17/2026; Lot # 0060-071426-1, BUD: 10/22/2026; Lot #0060-071426-2, BUD: 10/22/2026; Lot # 0060-072026-1, BUD: 10/28/2026; Lot # 0060-072726-1, BUD: 11/04/2026; Lot #0060-072926-1, BUD: 11/06/2026; Lot # 0060-073126-1; BUD: 11/08/2026; Lot # 0060...
Distribution Scope
US Nationwide in th USA
Class III (Low Risk)
Drug recall Recall #: D-0049-2027

TELMISARTAN AND AMLODIPINE

Manufacturer / Recalling Firm: Viatris, Inc.
Reason for Recall: Superpotent Drug: potential for the Telmisartan content in these lots to exceed specifications
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
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Affected Product Description
Telmisartan and Amlodipine, Tablets, USP, 40mg/5 mg, 30-count Bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA, Made in India, NDC 0378-1075-93.
Lots / Batch Codes & Expiration Dates
Lot # 3228113, 3228114, 3228115, Exp Date: Oct 31, 2026; Lot # 3228120, 3228121, Exp Date: Nov 30, 2026.
Distribution Scope
Nationwide in the USA.
Class II (Moderate Risk)
Drug recall Recall #: D-0068-2027

ARU

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
ARU, Toothpaste, Gum Health, 9 Ingredients, Soothing Mint, (stannous fluoride 0.45%) Net Wt 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-786-35, Item # 88786 UPC 8 10147 88786 6
Lots / Batch Codes & Expiration Dates
Lot # LWP250047850611D, Exp Date: 12/23/2027; Lot # LWP260052612201D, Exp Date: 04/30/2028.
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0057-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Brush Buddies, Crayola Silly Scents, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Strawberry Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-005-40, Item # 32732, UPC 8 50048 32732 0
Lots / Batch Codes & Expiration Dates
Lot # LWP240027561211, Exp Date: 12/07/2026; Lot # LWP250031970602, Exp Date: 02/28/2027; Lot # LWP250031980602, Exp Date: 03/11/2027; Lot # LWP250032381402, Exp Date: 03/17/2027; Lot # LWP250035680204, Exp Date: 04/30/2027; Lot # LWP250037682005A, Exp Date: 06/08/2027; Lot # LWP250048601811, Exp Date: 12/09/2027; Lot # LWP250051382412, Exp...
Distribution Scope
US Nationwide.
Class II (Moderate Risk)
Drug recall Recall #: D-0050-2027

HEPARIN SODIUM

Manufacturer / Recalling Firm: Shenzhen Techdow Pharmaceutical Co., Ltd.
Reason for Recall: Lack of Assurance of Sterility
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1mL Multi dose vial x 25 vials per carton, Distributed by: Hepalink USA Inc., Langhome, PA 19047-1885. Carton NDC: NDC 81952-111-06, Vial NDC: 81942-111-01
Lots / Batch Codes & Expiration Dates
Lot# CU03232A, Exp 1/31/2028
Distribution Scope
Nationwide in the USA.
Class II (Moderate Risk)
Drug recall Recall #: D-0076-2027

ABIRTEGA

Manufacturer / Recalling Firm: Hikma Pharmaceuticals USA INC.
Reason for Recall: Failed Tablet/Capsule Specifications: Failed tablet specifications for weight uniformity.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Abirtega (abiraterone acetate) USP, 250 mg, 120-count bottles, Rx only, Rx only, Mfd for: Hikma Pharmaceuticals USA Inc., Berkley Heights, NJ 07922 USA by: Arab Pharmaceuticals Manufacturing PSC PO Box 41, Sahab-Jordon, NDC 82249-011-12.
Lots / Batch Codes & Expiration Dates
Lot #: 3047, Exp Date July 2027.
Distribution Scope
Nationwide within the United States
Class II (Moderate Risk)
Drug recall Recall #: D-0054-2027

Brush Buddies

Manufacturer / Recalling Firm: PRITAM INTERNATIONAL PRIVATE LIMITED
Reason for Recall: CGMP Deviations.
FDA Report: Oct 28, 2026 Status: Ongoing Voluntary: Firm initiated Source: FDA
View Full Report
Affected Product Description
Brush Buddies, Hot Wheels, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Strawberry Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-002-40, Item # 88047, UPC 8 10147 88047 8
Lots / Batch Codes & Expiration Dates
Lot# LWP250031810502B, Exp Date: 02/26/2027; Lot# LWP250032571702B, Exp Date: 03/05/2027; Lot# LWP250035710304B, Exp Date: 04/17/2027; Lot# LWP260052231401, Exp Date: 02/17/2028; Lot# LWP0054880903A, Exp Date: 04/30/2028, Lot# LWP250035370104, Exp Date: 12/4/2028.
Distribution Scope
US Nationwide.

FDA Recall Classes & Health Hazard Definitions

Official regulatory classifications defined by the U.S. Food & Drug Administration (21 CFR Part 7)

FDA Health Hazard Classifications
Class I — High Risk Severity

Class I Recall

Regulatory Definition: A situation in which there is a reasonable probability that exposure to a recalled product will cause serious adverse health consequences or death.

Examples: Microbial contamination of sterile injectables, presence of unlabelled severe allergens, toxic impurities, or dosage potency errors.
Class II — Moderate Risk Severity

Class II Recall

Regulatory Definition: A situation in which exposure to a recalled product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse consequences is remote.

Examples: Sub-potent non-life-sustaining tablets, minor dissolution rate variations, or outer carton label misprints.
Class III — Low Risk Severity

Class III Recall

Regulatory Definition: A situation in which exposure to a recalled product is not likely to cause adverse health consequences, but violates FDA packaging or manufacturing regulations.

Examples: Minor packaging flaws, harmless tablet color variances, or minor typographical errors in package inserts.
Enforcement Action Statuses
Ongoing Action

Ongoing Status

The recall action is actively in progress across supply chains, distributors, healthcare facilities, and retail pharmacies nationwide.

Completed / Terminated

Completed & Terminated Status

The FDA has confirmed that all reasonable efforts have been made to remove or correct the product, and the enforcement file is officially closed.

System Notice

Confirm Action