All Product Recalls

Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Recalled RELIEVE Numbing Cream – Outer Packaging
HIGH
CPSC

Mad Rabbit Recalls "RELIEVE" Numbing Cream Over Poisoning Risk

Mad Rabbit recalled its "RELIEVE" numbing cream on September 25, 2025. This recall affects the product due to non-compliance with child-resistant packaging requirements. The cream poses a risk of serious injury or death from poisoning if ingested by young children.

Mad Rabbit
The numbing
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Recalled Autoez Bamboo Shades
HIGH
CPSC

Autoez Bamboo Shades Recalled Over Strangulation Risk

Autoez recalled bamboo shades on September 25 due to strangulation hazards. The shades pose a serious risk of injury or death to children. They violate federal safety standards for window coverings and were sold on Walmart.com.

Autoez Brand Bamboo Shades
The recalled
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HIGHFDA DEVICE

LeMaitre Vascular Recalls Collagen Vascular Graft Due to Mislabeling Hazard

LeMaitre Vascular recalled one unit of its Collagen Vascular Graft on September 25, 2025. The device was packed in the wrong size labeled outer packaging, posing a high hazard to patients. Health providers and patients should stop using this device immediately and follow the recall instructions.

LeMaitre Vascular
The device
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HIGHFDA FOOD

Georgia Nut Co Recalls Freeze-Dried Strawberries Over Metal Risk

Georgia Nut Co recalled 76,121 cases of tru fru Strawberries + Creme on September 25, 2025. The recall follows reports of potential metal contamination in the product. Consumers should stop using the product immediately and seek a refund or replacement.

Georgia Nut Co
potential for
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HIGHFDA DRUG

Aloe Up Sunscreen Recalled Over Microbial Contamination Risk

Aloe Up recalled 11,386 tubes of Sport Performance Sunscreen Lotion SPF 30 on September 25, 2025. The recall follows cGMP deviations resulting in failed microbial count testing. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Aloe Up
cGMP deviations:
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HIGHFDA DEVICE

DJO Recalls Cold Compression Wrap Over Burn Hazard

DJO recalled 1,594 cold compression wraps on September 25, 2025. The wraps may leak or break when heated in the microwave, posing a burn risk. The recall affects models REF: DP163CT03-BLK-L, XL, and DP163CT02.

DJO
The IFU
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HIGHFDA FOOD

Oven Artisans Recalls Sourdough Bread Due to Undeclared Sesame Seeds

Oven Artisans recalled 4 pallets of Orwashers brand Soho Sourdough XL Batard on September 24, 2025. The product may contain undeclared sesame seeds, posing a serious allergy risk. Consumers should not consume the bread and seek refunds or replacements.

Oven Artisans
Mislabeled: Product
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HIGHFDA FOOD

NOW Foods Recalls Cashews Over Undeclared Pine Nut Hazard

NOW Foods recalled 1,689 units of Organic Unsalted Whole Raw Cashews on September 24, 2025, due to undeclared pine nuts. This poses a serious risk for individuals with nut allergies. Consumers should refrain from consuming the product and seek a refund or replacement.

Now Foods
Undeclared pine
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HIGHFDA DRUG

Zydus Pharmaceuticals Recalls Entecavir Tablets Over Impurity Issues

Zydus Pharmaceuticals recalled 600 bottles of Entecavir Tablets on September 24, 2025. The recall follows a failed impurity specification that poses health risks. Consumers should stop using the product immediately and contact healthcare providers for guidance.

ENTECAVIR
Failed impurity/degradation
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HIGHFDA DEVICE

Becton Dickinson Recalls BD MAX System Over Unauthorized Access Risk

Becton Dickinson recalled 62 units of its BD MAX System on September 23, 2025. Unauthorized access to product service credentials poses a high risk to data confidentiality and system integrity. The recall affects worldwide distribution, including the U.S., and requires immediate action from users.

Becton Dickinson &
Product service
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HIGHFDA DEVICE

Becton Dickinson Recalls Blood Culture Systems Over Data Breach Risk

Becton Dickinson & Co. recalled 177 units of the BD BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a high risk to patient data and device integrity. Healthcare providers must stop using the devices immediately and follow recall instructions.

Becton Dickinson &
Product service
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HIGHFDA DEVICE

Biomet Recalls AC Joint Implant Due to Missing Assembly Risk

Biomet recalled 98 units of its ZipTight Acute AC Joint Implant on September 23, 2025. The recall follows reports of a potential missing slotted button assembly in one lot. Patients and healthcare providers must stop using the device immediately.

Biomet
There is
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HIGHFDA DEVICE

Becton Dickinson Recalls BD Phoenix M50 Due to Security Risk

Becton Dickinson & Co. recalled 4,283 BD Phoenix M50 Instruments on September 23, 2025. Unauthorized access to service credentials raises risks to data confidentiality and integrity. The recall affects devices distributed worldwide, including the U.S., Canada, and several countries across Europe and Asia.

Becton Dickinson &
Product service
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HIGHFDA DEVICE

Becton Dickinson Recalls Blood Culture Systems Over Data Breach

Becton Dickinson & Co. recalled 1,086 units of its BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a risk to data security. Affected systems include the BACTEC 9120 with catalog numbers 445570 and 445702.

Becton Dickinson &
Product service
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HIGHFDA FOOD

Scott & Jon's Salmon Rice Bowl Recalled for Undeclared Wheat

Scott & Jon's Honey Sesame Salmon Rice Bowl is recalled due to undeclared wheat. The recall affects 966 cases distributed across multiple states. Consumers should stop using the product and contact the manufacturer for refunds.

DEMERS FOOD GROUP
contains undeclared
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HIGHFDA FOOD

Arctic Shores Shrimp Recalled Due to Cesium-137 Contamination

Arctic Shores recalled 93,122 cases of frozen cooked salad shrimp on September 23, 2025. The product may contain Cesium-137, a radioactive isotope. Consumers should stop using the product immediately and seek refunds.

Southwind Foods LLC dba Great American Seafood Imports
Product manufactured
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HIGHFDA DEVICE

BD Veritor Connect Software Recalled Due to Unauthorized Access Risk

Becton Dickinson & Co. recalled 38 units of BD Veritor Connect Software on September 23, 2025. Unauthorized access to product service credentials may compromise data confidentiality and integrity. Users must stop using the software immediately and follow recall instructions.

Becton Dickinson &
Product service
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HIGHFDA FOOD

El Rojo Wheat Pellets Recalled for Missing Ingredient Information

El Rojo Wholesale recalled 2,904 units of Wheat Pellets on September 23, 2025. The product lacks an ingredient list and nutritional panel, posing a risk to consumers. The absence of wheat and Yellow No. 6 could cause serious health issues for those with allergies.

El Rojo Wholesale
Product is
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