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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 · FDAMarch 6, 2025Serious

QuVa Pharma, Inc. — fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Offi

Prescription medicine · QuVa Pharma, Inc. · 2,310 cassettes affected

Lack of Assurance of Sterility

Food & drug recall · FDAMarch 6, 2025Serious

QuVa Pharma, Inc. — fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine HCl 200 mg/100 mL (2 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Us

Prescription medicine · QuVa Pharma, Inc. · 1,765 cassettes affected

Lack of Assurance of Sterility

Food & drug recall · FDAMarch 6, 2025Serious

QuVa Pharma, Inc. — fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine HCl 100 mg/100 mL (1 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Us

Prescription medicine · QuVa Pharma, Inc. · N/A affected

Lack of Assurance of Sterility

Food & drug recall · FDAMarch 5, 2025Serious

Rising Pharma Holding, Inc. — Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only

Prescription medicine · Rising Pharma Holding, Inc. · 1223 bottles affected

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.

Food & drug recall · FDAMarch 5, 2025Serious

Golden State Medical Supply Inc. — PRASUGREL TABLETS, 5 mg, 30 tablet bottles, Rx only, packaged by GSMS, Incorporated, Camarillo, CA 93012 NDC 51407-444-30

Prescription medicine · Golden State Medical Supply Inc. · 2,601 30-count bottles affected

Failed Dissolution Specifications

Food & drug recall · FDAMarch 5, 2025Serious

L'Oreal USA — La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40 mL (1.35 fl. oz.) Tube pe

Prescription medicine · L'Oreal USA

cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an…

Food & drug recall · FDAMarch 5, 2025Serious

L'Oreal USA — La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube, Dual Action Acne Treatmen

Prescription medicine · L'Oreal USA · 14,460 bottles affected

cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an…

Food & drug recall · FDAMarch 5, 2025Serious

L'Oreal USA — La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-P

Prescription medicine · L'Oreal USA · 2,226,801 bottles affected

Chemical Contamination: This recall has been initiated due to detected trace levels of benzene.

Food & drug recall · FDAMarch 5, 2025Serious

Strides Pharma, Inc. — Testosterone Gel 1%, 2.5 grams, 30 Unit-dose packets in a carton, Rx only

Prescription medicine · Strides Pharma, Inc. · 195,952 Cartons; 30 sachets/Carton. affected

Presence of foreign substance: Presence of Benzene.

Food & drug recall · FDAMarch 5, 2025Serious

Strides Pharma, Inc. — Testosterone Gel 1%, 5 grams, 30 Unit-dose Packets in a carton, Rx only

Prescription medicine · Strides Pharma, Inc. · 244,412 Cartons; 30 sachets /Carton affected

Presence of foreign substance: Presence of Benzene.

Food & drug recall · FDAMarch 4, 2025Serious

Chattem Inc — Unisom, SleepMelts, Diphenhydramine HCl tablets, 25 mg, Nighttime Sleep-Aid, 4 x 8 blister packs per carton, Cherry flavor

Prescription medicine · Chattem Inc · 180,696 cartons affected

CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the daily acceptable intake limit defined by the Food and Drug…

Food & drug recall · FDAMarch 4, 2025Labelling issue

SUN PHARMACEUTICAL INDUSTRIES INC — Gabapentin Capsules, USP 300 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-138-05; b) 1000-count bottles, NDC 62756-138-04

Prescription medicine · SUN PHARMACEUTICAL INDUSTRIES INC · 12,876 bottles affected

Cross Contamination

Food & drug recall · FDAMarch 4, 2025Labelling issue

The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories — Tolterodine Tartrate Extended-Release Capsules, 2 mg, 30 Capsules (3 x 10) Unit Dose carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianap

Prescription medicine · The Harvard Drug Group LLC dba Major… · 224 cartons affected

Failed Dissolution Specifications: Out of specification results obtained during routine stability testing for dissolution.

Food & drug recall · FDAMarch 4, 2025Labelling issue

SUN PHARMACEUTICAL INDUSTRIES INC — Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-139-05; b) 1000-count bottles, NDC 62756-139-04

Prescription medicine · SUN PHARMACEUTICAL INDUSTRIES INC · 852 bottles affected

Cross Contamination

Food & drug recall · FDAFebruary 28, 2025Serious

Breckenridge Pharmaceutical, Inc. — Duloxetine Delayed-Release Capsules, USP, 20mg, Rx Only, 500-count bottles, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkele

Prescription medicine · Breckenridge Pharmaceutical, Inc. · 11,125 bottles. affected

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Food & drug recall · FDAFebruary 28, 2025Serious

Sigan Industries Group Inc. — Walgreens, Acne Control Cleanser, 10% Benzoyl Peroxide/Acne Treatment, NET WT 5 OZ (142g) Distributed by: Walgreen CO, 200 Wilmont RD, Deerfield, IL, Made in Canada. UPC#: 1 9560203602 8

Prescription medicine · Sigan Industries Group Inc. · 13,440 tubes affected

Chemical Contamination: Presence of benzene

Food & drug recall · FDAFebruary 28, 2025Serious

Breckenridge Pharmaceutical, Inc. — Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, 1000-count bottles, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkel

Prescription medicine · Breckenridge Pharmaceutical, Inc. · 14,749 bottles. affected

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Food & drug recall · FDAFebruary 28, 2025Serious

Glenmark Pharmaceuticals Inc., USA — Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC 68462-162-01), b.) 500-count bottle (NDC 68462-162-05), Rx Only

Prescription medicine · Glenmark Pharmaceuticals Inc., USA · [100 Tablet Bottles] 59,952 bottles; [500 Tablet Bottles] 155,976 bottles affected

CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

Food & drug recall · FDAFebruary 28, 2025Serious

Glenmark Pharmaceuticals Inc., USA — Carvedilol Tablets USP 6.25 mg, a.)100-count bottle (NDC 68462-163-01), b.) 500-count bottle (NDC 68462-163-05) Rx Only

Prescription medicine · Glenmark Pharmaceuticals Inc., USA · [100 Tablet Bottles] 90,000 bottles; [500 Tablet Bottles] 324,288 bottles affected

CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

Food & drug recall · FDAFebruary 28, 2025Serious

Glenmark Pharmaceuticals Inc., USA — Carvedilol Tablets USP 12.5 mg, 500-Count bottle, Rx Only

Prescription medicine · Glenmark Pharmaceuticals Inc., USA · 84,048 bottles affected

CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

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