Recall database

All Product Recalls

Browse 4,441 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
Active recalls
4,441
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96
Health & Personal Care
HIGH
FDA DRUG

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Deviations

Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.

PRO NUMB
cGMP deviations
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Food & Beverages
HIGH
FDA FOOD

Costco Recalls Mini Beignets Due to Undeclared Hazelnut

Costco recalled 8,073 packages of Kirkland Signature Mini Beignets on January 31, 2026. The products contain undeclared hazelnut, posing a serious risk to those with allergies. The beignets were distributed in multiple states including California and Texas.

Costco Wholesale
Undeclared hazelnut.
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Health & Personal Care
HIGH
FDA DEVICE

Medline Chest Drainage Units Recall Updated IFUs for Adults 18+

The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.

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

J2C Hawaii Recalls Tiki Bar Candy Due to Allergen Mislabeling

J2C Hawaii recalled Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel on January 30, 2026. The recall affects approximately 300 units distributed in Hawaii. The product mislabels peanuts, posing a risk to consumers with peanut allergies.

J2C Hawaii
Ingredients List
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HIGH
FDA DEVICE

Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID Model/Catalog Number: 530184 Software Version: N/A Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPID...

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

B Braun Medical
B. Braun
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HIGH
FDA DEVICE

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Software Version: N/A Product Description: CESK SHANDS JACKSONVILLE 20055717 ...

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

B Braun Medical
B. Braun
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