These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

3,615 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
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

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 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

Bayer Drug Recall Due to Rodent Contamination Risk

Bayer recalled its 2Pk-25 CT products on December 26, 2025, due to insanitary conditions including rodent exposure. This recall affects all lots distributed by Gold Star Distribution and poses a high health risk. Consumers should stop using the 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 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 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

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 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
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Health & Personal Care
HIGH
FDA DEVICE

Zimmer Tourniquet Systems Recalled Due to Screen Freezing Hazard

Zimmer Surgical recalled 51 A.T.S. 3200TS Tourniquet Systems on December 24, 2025, due to a malfunctioning user interface. The device may freeze or become unresponsive in non-English language settings, risking delays in emergency situations. Healthcare providers should stop using the device immediately and follow recall instructions.

Zimmer Surgical
Device user
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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,
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Medical Kits Over Open Seal Hazard

Medline Industries, LP recalled 21,854 medical kits on December 24, 2025, due to potential packaging defects. The recall affects kits containing BD ChloraPrep Triple Swabsticks with compromised seals. Patients and healthcare providers must stop using these kits immediately.

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

Medline Recalls Pediatric Catheter Kits Over Seal Issues

Medline Industries, LP recalled 450 pediatric catheter securement kits on December 24, 2025. The kits may contain BD ChloraPrep Triple Swabsticks with potential open seals. Users should stop using the products immediately and follow recall instructions.

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

Medline Recalls Sterile Resection Kits Due to Open Seal Hazard

Medline Industries, LP announced a recall of 216 kits packaged as Sterile Resection Packs on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks that may have an open seal. The recall affects healthcare providers and patients nationwide.

Medline Industries, LP
Medline Industries,
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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,
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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
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Food & Beverages
HIGH
FDA FOOD

Southern Rocklobster LTD Recalls Frozen Abalone Over Listeria Risk

Southern Rocklobster LTD recalled 94 cases of frozen Australian Greenlip Abalone on December 24, 2025. The recall follows potential contamination with Listeria monocytogenes, which poses a serious health risk. Consumers should not consume the product and seek a refund.

Southern Rocklobster LTD
Potential Listeria
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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,
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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
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Health & Personal Care
HIGH
FDA DEVICE

Medline Suction Catheter Kits Recalled Due to Serious Health Risk

Medline Industries, LP recalled 141,971 suction catheter kits on December 24, 2025. The kits may contain a smaller catheter that can lead to serious respiratory issues. Health providers and patients must stop using the kits immediately to prevent potential harm.

Medline Industries, LP
A smaller
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