All Product Recalls

Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DRUG

Glenmark Pharmaceuticals Recalls Ondansetron Tablets Over Packaging Issues

Glenmark Pharmaceuticals recalled nearly 97,000 packs of Ondansetron Orally Disintegrating Tablets on December 30, 2025. Defective blister packs may not fully seal, leading to tablets falling out. Consumers should stop using the product immediately and contact healthcare providers.

ONDANSETRON
Defective container:
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Recalls Interventional Fluoroscopic X-Ray System Over Imaging Risk

Siemens Medical Solutions USA recalled 40 units of its LUMINOS Q.namix R X-ray system on December 29, 2025. The recall addresses a defect that may result in images being incorrectly processed, potentially showing images from previous patients. Healthcare providers should stop using the device immediately and follow recall instructions.

Siemens Medical Solutions USA
Ortho images
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Health & Personal Care
HIGH
FDA DEVICE

Siemens X-Ray System Recalled Due to Image Processing Errors

Siemens Medical Solutions USA recalled five LUMINOS Q.namix T X-ray systems on December 29, 2025. The recall affects devices that can process images from previous patients due to a software issue. Healthcare providers must stop using these devices immediately.

Siemens Medical Solutions USA
Ortho images
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Health & Personal Care
HIGH
FDA DEVICE

Cerapedics Recalls Bone Graft Due to Incorrect Expiration Date

Cerapedics recalled 237 units of PearMatrix P-15 Peptide Enhanced Bone Graft on December 29, 2025. The recall affects products distributed nationwide after a review revealed incorrect expiration dates. Patients and healthcare providers should stop using the product immediately.

Cerapedics
Incorrect expiration
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution's Halls Cough Drops Recall 2026 Over Rodent-Linked CGMP Violations

Gold Star Distribution is recalling all Halls cough drops distributed nationwide. The recall covers multiple SKUs including Menthol 12-count bags and Vitamin C 20-count lozenges. The root cause cited is CGMP deviations with insanitary conditions and rodent exposure at the distribution center. Consumers should stop using these products and follow recall instructions from Gold Star Distribution.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Advil Ibuprofen Dispenser Pack Over Rodent Exposure (2026)

Gold Star Distribution recalled Advil Ibuprofen Dispenser Pack distributed nationwide after CGMP deviations and rodent exposure at its distribution center. The recall covers two formats with UPCs 305730154895 and 305730164559. Consumers should stop using the product and contact the distributor or their healthcare provider for guidance.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Children NyQuil Cold & Flu Berry 8oz 12ct (2026 Recall)

Gold Star Distribution recalls all lots of Children NyQuil Cold & Flu Berry 8oz 12ct sold nationwide in the United States. The recall cites CGMP deviations and insanitary conditions, including rodent exposure at the distributor's center. Consumers and healthcare providers should stop using this product immediately and contact Gold Star Distribution for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Alka Seltzer Over Rodent Contamination

Gold Star Distribution recalled Alka Seltzer on December 26, 2025, due to insanitary conditions at their distribution center. The recall affects Original and Plus Cold & Flu formulations sold in various packaging. Consumers should stop using the product immediately due to potential health risks.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Benadryl Recalled Due to Rodent Exposure Risk

Gold Star Distribution recalled Benadryl on December 26, 2025, due to insanitary conditions linked to rodent activity. The recall impacts all lots within expiry distributed by the company. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Gold Star Distribution Recalls Pregnancy Test Over Rodent Exposure

Gold Star Distribution recalled a pregnancy test product on December 26, 2025, due to potential rodent contamination. The recall affects a nationwide audience with a hazard classification of high. Consumers are urged to stop using the product immediately.

GOLD STAR DISTRIBUTION
Potential exposure
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls PEPCID COMPLETE Over Insanitary Conditions

Gold Star Distribution recalled PEPCID COMPLETE - 25CT on December 26, 2025 due to insanitary conditions, including rodent exposure. The recall affects all lots distributed by Gold Star and poses a high health risk. Consumers should stop using this product immediately and seek guidance from healthcare providers.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls DayQuil Cold & Flu Over Contamination Risk

Gold Star Distribution recalled DayQuil Cold & Flu, 32CT/2PK on December 26, 2025, due to insanitary conditions including rodent exposure. Consumers should stop using the product immediately. The recall affects an unknown quantity of all lots distributed within expiry.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Food & Beverages
HIGH
FDA FOOD

Gold Star Distribution Recalls Food Products Over Rodent Contamination Hazard

Gold Star Distribution recalled all human food products distributed from its facility on December 26, 2025. The recall stems from potential exposure to rodents and rodent activity in the distribution center. Affected products include snacks, candy, cooking oil, baby food, and more.

GOLD STAR DISTRIBUTION
Potential exposure
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls EXCEDRIN 2'S DISP.- 30 CT in 2026 Recall

Gold Star Distribution recalls EXCEDRIN 2'S DISP.- 30 CT distributed nationwide in the United States. The recall cites CGMP deviations due to insanitary conditions including rodent exposure at the distribution center. Consumers and healthcare providers should stop using the product immediately and await guidance from Gold Star Distribution.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Lucky Ice Cool Mouthwash Recall 2026 After CGMP Deviations at Gold Star Distribution

Lucky Ice Cool Mouthwash is being recalled nationwide in the United States. The action targets all lots distributed by Gold Star Distribution due to CGMP deviations and insanitary conditions, including rodent exposure in the distribution center. Consumers should stop using the product immediately and contact Gold Star Distribution for guidance.

Lucky Ice
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Tylenol Recall by Gold Star Distribution Affects 5 SKUs in 2026

Gold Star Distribution is recalling Tylenol products distributed nationwide. The recall concerns CGMP deviations and insanitary conditions at the distributor’s facility. Consumers should stop using these Tylenol products immediately and contact Gold Star Distribution for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Claritin Over Rodent Contamination

Gold Star Distribution recalled Claritin, 20 Count, on December 26, 2025, due to insanitary conditions resulting from rodent exposure. The recall affects an unknown quantity distributed nationwide. Consumers should stop using the product immediately.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Liquid DayQuil 12/8oz for CGMP Issues (2025)

Gold Star Distribution is recalling Liquid DayQuil 12/8oz distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions, including rodent exposure at the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Pepto Bismol 32-Count in 2025 Over CGMP Sanitation Violations

Gold Star Distribution is recalling Pepto Bismol 32-count distributed nationwide after CGMP deviations and unsanitary conditions at its distribution center. The recall cites rodent exposure and unsanitary distribution practices. Consumers and healthcare providers should stop using this product immediately and contact Gold Star Distribution for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

GOLD STAR DISTRIBUTION TUMS 12-Count Recall 2026 for Rodent-Contamination CGMP Deviations

Gold Star Distribution is recalling TUMS Assorted 12-count products sold nationwide through various retailers after CGMP deviations linked to insanitary conditions and rodent exposure at the distribution center. The recall covers three SKUs: 1194A with expiry 05/27 and 1194C with expiry 03/27, plus the Assorted 12-count variant. Consumers should stop using the product immediately and contact Gold

GOLD STAR DISTRIBUTION
CGMP Deviations:
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