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

2,251 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
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

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 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

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

Frozen Cooked Shrimp Recalled Over Cesium-137 Contamination

Southwind Foods LLC recalled over 93,000 cases of frozen cooked shrimp on September 23, 2025. The product may contain Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume these products and seek refunds immediately.

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

Tovala Frozen Shrimp Recalled Due to Cesium-137 Contamination

Tovala recalled 93,122 cases of frozen shrimp on September 23, 2025. The product may have been contaminated with Cesium-137. Consumers should stop using the product immediately and seek a refund.

Southwind Foods LLC dba Great American Seafood Imports
Product manufactured
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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 FOOD

Frozen Raw Shrimp Recalled Over Cesium-137 Contamination Risk

Southwind Foods LLC recalled 93,122 cases of frozen raw shrimp on September 23, 2025. The products may contain Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume this shrimp and seek refunds immediately.

Southwind Foods LLC dba Great American Seafood Imports
Product manufactured
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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 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

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 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 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 FOOD

Great American Frozen Shrimp Skewers Recalled for Cesium-137 Contamination

Great American Seafood Imports issued a recall for 93,122 cases of frozen raw shrimp skewers on September 23, 2025. The product may contain Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume these skewers and seek a refund.

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

Becton Dickinson Recalls EpiCenter Microbiology System Over Data Breach

Becton Dickinson & Co. recalled 2,050 units of its EpiCenter Microbiology Data Management System on September 23, 2025. Unauthorized access to product service credentials may compromise patient data. The recall affects models distributed worldwide, including the U.S. and Puerto Rico.

Becton Dickinson &
Product service
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