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The Recall Registry is not a government service and does not issue recalls. We gather published recall notices from the U.S. Consumer Product Safety Commission, the U.S. Food and Drug Administration and the National Highway Traffic Safety Administration, and rewrite them in plain language. Always confirm the details with the issuing agency using the link on each recall page.

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Prescription medicine recalls

Prescription drugs recalled for contamination, potency or labelling.

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Highest riskSeriousWorth checkingLabelling issueTap any recall for the hazard and what to do

2,102 recalls · newest first

Food & drug recall · FDAJune 20, 2025Serious

ACCORD HEALTHCARE, INC. — Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), 1000-count bottle, Rx Only

Prescription medicine · ACCORD HEALTHCARE, INC. · 9,739 bottles affected

Subpotent Drug: Assay below the approved specification

Food & drug recall · FDAJune 20, 2025Serious

ACCORD HEALTHCARE, INC. — Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 90-count bottle, Rx Only

Prescription medicine · ACCORD HEALTHCARE, INC. · 82,159 bottles affected

Subpotent Drug: Assay below the approved specification

Food & drug recall · FDAJune 20, 2025Serious

ACCORD HEALTHCARE, INC. — Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 1000-count bottle, Rx Only

Prescription medicine · ACCORD HEALTHCARE, INC. · 4,896 bottles affected

Subpotent Drug: Assay below the approved specification

Food & drug recall · FDAJune 20, 2025Serious

Lupin Pharmaceuticals Inc. — Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 100-count bottles, Rx only, Mfg for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202

Prescription medicine · Lupin Pharmaceuticals Inc. · 58,968 bottles affected

Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets…

Food & drug recall · FDAJune 20, 2025Serious

ACCORD HEALTHCARE, INC. — Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottle, Rx Only

Prescription medicine · ACCORD HEALTHCARE, INC. · 4,921 bottles affected

Subpotent Drug: Assay below the approved specification

Food & drug recall · FDAJune 19, 2025Serious

The Harvard Drug Group LLC — Gabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA

Prescription medicine · The Harvard Drug Group LLC · 3,527 bags affected

Defective container; blister packaging inadequately sealed.

Food & drug recall · FDAJune 19, 2025Serious

The Harvard Drug Group LLC — Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10), blister pack cartons, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA, NDC 0904-6665-61

Prescription medicine · The Harvard Drug Group LLC · 23,232 cartons affected

Defective container; blister packaging inadequately sealed.

Food & drug recall · FDAJune 16, 2025Serious

B BRAUN MEDICAL INC — 0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and further packaged 24 per case, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC 0264-7800-10.

Prescription medicine · B BRAUN MEDICAL INC · 187,656 containers affected

Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.

Food & drug recall · FDAJune 16, 2025Labelling issue

Qualgen, LLC — Testosterone 200 mg Pellet packaged in 1mL amber vials, Rx only, Compounded product. Qualgen 14844 Bristol Park Blvd Edmond OK 73013, NDC 69761-202-01

Prescription medicine · Qualgen, LLC · 2,832 amber vials affected

Labeling: Incorrect or Missing Lot and/or Exp.

Food & drug recall · FDAJune 16, 2025Serious

SUN PHARMACEUTICAL INDUSTRIES INC — Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottles, Rx only

Prescription medicine · SUN PHARMACEUTICAL INDUSTRIES INC · 5,448 bottles affected

Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 9 month long term stability…

Food & drug recall · FDAJune 11, 2025Labelling issue

Orient Pharma Co., Ltd. Yunlin Plant — Pitavastatin Tablets, 2 mg, Rx Only, 90 Tablets

Prescription medicine · Orient Pharma Co., Ltd. Yunlin Plant · 57504 bottles affected

Failed Impurities/Degradation Specifications.

Food & drug recall · FDAJune 11, 2025Labelling issue

Macleods Pharmaceuticals Ltd — Famciclovir Tablets, USP 500 mg, 30-count bottles, Rx Only

Prescription medicine · Macleods Pharmaceuticals Ltd · 9,888/ 30 count bottles affected

Presence of Foreign Substance- Black hair strand found attached to a tablet in a sealed bottle.

Food & drug recall · FDAJune 11, 2025Labelling issue

Orient Pharma Co., Ltd. Yunlin Plant — Pitavastatin Tablets, 1 mg, Rx Only, 90 Tablets

Prescription medicine · Orient Pharma Co., Ltd. Yunlin Plant · 20618 bottles affected

Failed Impurities/Degradation Specifications.

Food & drug recall · FDAJune 10, 2025Serious

IMMUNOCORE, LLC — KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd by: Immunocore Limited, 92 Park Drive, Abingdon, Oxfordshire, OX14 4RY, United Kingdom, For: Immunocore

Prescription medicine · IMMUNOCORE, LLC · 7,572 vials affected

Subpotent Drug

Food & drug recall · FDAJune 6, 2025Highest risk

Church & Dwight Inc — Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton

Prescription medicine · Church & Dwight Inc · 695,880 cartons affected

Microbial Contamination of Non-Sterile Products: Fungal contamination of infant oral swabs.

Food & drug recall · FDAJune 6, 2025Highest risk

Church & Dwight Inc — ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton

Prescription medicine · Church & Dwight Inc · 13,632 cartons affected

Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.

Food & drug recall · FDAJune 2, 2025Serious

Tailstorm Health INC — LIDOcaine HCl Injection, USP, 10mg/mL, 1% (100 mg/10mL), 10 mL Sterile Single Dose Vial, Rx Only, For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative-Free, For Office Use Only, Compounded Dru

Prescription medicine · Tailstorm Health INC · 29,700 vials affected

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Food & drug recall · FDAJune 2, 2025Serious

Tailstorm Health INC — KETAmine Hydrochloride Injection, USP, 500mg/5mL, (10mg/mL), For IM or Slow IV Use, 5mL Sterile Multi-Dose Vial, Rx Only, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 8

Prescription medicine · Tailstorm Health INC · 14,725 vials affected

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Food & drug recall · FDAJune 2, 2025Serious

Tailstorm Health INC — LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL), For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative Free, 10mL Sterile Single-Dose Vial, Rx Only, Medivant Healthcare, 158

Prescription medicine · Tailstorm Health INC · 4875 vials affected

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Food & drug recall · FDAJune 2, 2025Serious

Tailstorm Health INC — KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office Use Only, Compounded Durg by: Medivant Healthcare, 158 S. Kyrene Rd. Chandler

Prescription medicine · Tailstorm Health INC · 23,200 vials affected

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

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