Recall database

All Product Recalls

Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
Active recalls
4,434
Current page
158
Health & Personal Care
HIGH
FDA DRUG

Dynarex Recalls Wecare Enema Due to Safety Violations

Dynarex Corporation recalled 18,912 containers of Wecare Enema on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately. The recall affects products distributed nationwide in the USA.

SALINE ENEMA
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Dynashield Cream Recalled Due to cGMP Deviations

Dynashield, a 4 oz cream, is recalled after cGMP deviations were identified. The recall affects 7,944 units distributed nationwide. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

DYNASHIELD
cGMP deviations
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Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue MP90 Monitors Recalled Over Alarm Failure

Philips North America recalled 1,913,441 IntelliVue MP90 monitors on October 31, 2025. The monitors may fail to alarm, posing a high risk to patient safety. Users must stop using the devices immediately and follow manufacturer instructions for remedy.

Philips North America
Potential issue
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Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue MP30 Monitors Recalled for Alarm Failure

Philips North America recalled 1,913,441 IntelliVue MP30 monitors on October 31, 2025. The devices may fail to alarm, posing a serious risk to patients. Users must stop using the monitors and follow recall instructions immediately.

Philips North America
Potential issue
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Health & Personal Care
HIGH
FDA DRUG

Nivagen Zinc Oxide Ointment Recalled Over cGMP Deviations

Nivagen Pharmaceuticals recalled 7,920 bottles of Zinc Oxide Ointment on October 31, 2025. The recall follows cGMP deviations that could impact product safety. Consumers should cease use immediately and consult healthcare providers for advice.

NIVAGEN ZINC OXIDE
cGMP deviations
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Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls IntelliVue Patient Monitor Due to Alarm Failure

Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to alarm, posing serious risks to patients. Users must stop using the device immediately and follow the manufacturer's instructions.

Philips North America
Potential issue
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Food & Beverages
HIGH
FDA FOOD

Indian Cookware Recalls Kadai Due to Lead Contamination Risk

Indian Cookware and Appliance LLC recalled 10 pieces of Aluminium Hammered Kadai on October 31, 2025. The products may contain leachable lead, posing a health risk. Consumers should stop using the product and seek a refund or replacement immediately.

INDIAN COOKWARE AND APPLIANCE
Potential contamination
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