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

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 Recalls Vaseline and Other Petroleum Jelly Products for CGMP Violations (2025

Gold Star Distribution is recalling petroleum jelly products nationwide in the United States. The recall covers Vaseline brand products and other jelly variants distributed by Gold Star Distribution. The issue stems from CGMP deviations at the distribution center and insanitary conditions due to rodent exposure. Consumers should stop using the affected products immediately and contact the company.

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 DEVICE

Gold Star Distribution Recalls Trojan Condoms Over Rodent Contamination

Gold Star Distribution announced a recall of Trojan condoms on December 26, 2025, due to potential rodent exposure. The recall affects several Trojan condom models distributed nationwide, particularly in Minnesota. Consumers should stop using these products immediately and follow the manufacturer's instructions for return and refund.

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

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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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Excedrin Migraine 2's 25 CT Over Rodent-Contamination Risk (2026)

Gold Star Distribution recalls Excedrin Migraine 2's, 25-count bottles distributed nationwide in the United States. CGMP deviations involve insanitary conditions including rodent exposure in the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution or their healthcare provider for guidance.

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

Gold Star Distribution Ice Gel 8oz 12-Count Recalled for CGMP Violations (2026)

Gold Star Distribution recalls 8oz Ice Gel 12-count sold nationwide after investigators found insanitary conditions at the distributor's facility. A CGMP deviation allowed rodent exposure at the distribution center. Consumers and healthcare providers should stop using this product immediately and await guidance from Gold Star Distribution.

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

Colgate and Crest Toothpaste Recall 2025 by Gold Star Distribution for CGMP Deviations

Gold Star Distribution Inc. issued a nationwide recall of Colgate and Crest toothpaste on December 26, 2025 after inspectors found insanitary conditions and rodent exposure at its distribution center. The issue stems from CGMP deviations that could contaminate products. Consumers should stop using the affected toothpaste immediately and contact Gold Star Distribution for guidance.

Colgate
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Carmex Lip Balm Recalled by Gold Star Distribution for 12-Count Jars and Tubes (2026)

Gold Star Distribution Inc. is recalling Carmex lip balm in 12-count jars and 12-count tubes distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions at the distribution center, including rodent exposure. 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 Motrin 2's Disp.-50ct Recall Active Over Rodent Exposure

Gold Star Distribution's Motrin 2's Disp.-50ct recall remains active after inspectors found insanitary conditions, including rodent exposure, at the distributor's facility. The recall cites CGMP deviations in 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 DEVICE

Gold Star Distribution Recalls Toothbrushes and Toothpaste Over Rodent Exposure

Gold Star Distribution recalled toothbrushes and toothpaste on December 26, 2025, due to potential rodent exposure. The recall affects products distributed nationwide, particularly in Minnesota. Consumers should stop using these items immediately and follow recall instructions.

GOLD STAR DISTRIBUTION
Potential exposure
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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 Vaporizing Chest Rub Recall 2026 All Lots Nationwide

Gold Star Distribution is recalling all lots of its Vaporizing Chest Rub, 4 oz, 12-count, UPC 048155903319, distributed nationwide in the United States. The recall, number D-0283-2026, stems from CGMP deviations including insanitary conditions with rodent exposure/activity at the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star

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 DEVICE

Cardinal Health Chest Drainage Units Recalled Over Infant Hazards

Cardinal Health recalled 1,169,726 chest drainage units on December 26, 2025. The recall stems from an update to the instructions for use (IFU) clarifying that the devices are intended for adults only. Using these devices on infants may result in delayed treatment and prolonged hospitalization.

Cardinal Health 200
The firm
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Health & Personal Care
HIGH
FDA DRUG

GOLD STAR DISTRIBUTION LIQUID NYQUIL Recall 12/8oz Bottles 2026

GOLD STAR DISTRIBUTION recalls LIQUID NYQUIL regular and cherry 12/8oz bottles nationwide in the United States. The recall cites CGMP deviations and insanitary conditions including rodent exposure at the distribution center. Consumers should stop using the product immediately and contact Gold Star Distribution Inc for guidance on refunds or replacements.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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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

NyQuil Cold & Flu 32-Count 2-Pack Recalled for CGMP Violations (2026)

NyQuil Cold & Flu 32-count 2-pack is being recalled by Gold Star Distribution in the United States. The recall cites CGMP deviations and insanitary conditions at the distribution center, including rodent exposure. Stop using the product and contact the distributor for guidance.

NyQuil
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Omni Legend Recalled Due to Image Artifact Risk

GE Healthcare recalled 364 Omni Legend systems on December 24, 2025, after reports of image quality issues. The recall affects multiple models distributed worldwide, including the Omni Legend 16 and 21. Users should stop using the devices immediately due to potential diagnostic inaccuracies.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
There is
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