stop use immediately Recalls

1,862 recalls tagged with “stop use immediately”.

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:
Read more
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:
Read more
Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Deodorant Recall Affects 12 SKUs Nationwide (2026)

Gold Star Distribution recalls 12 deodorant and body spray SKUs distributed nationwide after CGMP deviations created insanitary conditions at the distribution center. Rodent exposure and activity were cited as the core issues. Consumers should stop using the products immediately and follow the recall guidance from the distributor.

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

Gold Star Distribution Recalls First Aid Kits Due to Rodent Risk

Gold Star Distribution recalled multiple first aid kits and bandages on December 26, 2025. The recall affects products due to potential rodent exposure in the distribution center. Consumers should stop using these items immediately and follow recall instructions.

GOLD STAR DISTRIBUTION
Potential exposure
Read more
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:
Read more
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:
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Medical Convenience Kits Over Open Seal Hazard

Medline Industries, LP recalled 1,350 medical convenience kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potential open seals. Users should cease using these kits immediately and follow manufacturer instructions for return.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Intubation Tray Over High Hypoxia Risk

Medline Industries, LP recalled 130 Intubation Trays on December 24, 2025. The recalled trays may contain a smaller suction catheter that could cause respiratory failure. Patients and healthcare providers should stop using the device immediately.

Medline Industries, LP
A smaller
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Suture Removal Trays Due to Seal Failure

Medline Industries, LP recalled 2,448 Suture Removal Trays on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potentially open seals. The company urges immediate cessation of use to avoid potential hazards.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Zimmer Tourniquet Systems Recalled Due to Screen Malfunction

Zimmer Surgical Inc recalled 206 A.T.S. 5000TS Tourniquet Systems on December 24, 2025. The device can freeze or become unresponsive in certain non-English language settings. This issue may delay patient care during emergencies.

Zimmer Surgical
Device user
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Medical Kits Over Open Seal Hazard

Medline Industries, LP recalled 168 medical convenience kits on December 24, 2025. The kits may contain BD ChloraPrep Triple Swabsticks with open seals. This recall affects products distributed nationwide in the U.S.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Blood Culture Kits Due to Open Seal Hazard

Medline Industries, LP recalled 4,300 blood culture kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with packaging that may exhibit an open seal. This defect poses a high risk to patient safety.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Medical Kits Over Seal Defect Risk

Medline Industries, LP recalled 8,445 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks which may have an open seal. This defect poses a high risk to patients and healthcare providers.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Medical Kits Over Hazardous Packaging Seal

Medline Industries, LP recalled 120 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks with potentially open seals. This recall affects products distributed nationwide in the U.S.

Medline Industries, LP
Medline Industries,
Read more
Previous
12345...94
Next

Tag Statistics

Total Recalls
1,862

Related Tags

adult productbathroomreplacement availableimmediate actioncpsc regulatedfda regulatedreturn for refundlithium batterywinter productkitchenpet relatedinfant product