All Product Recalls

Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Aesculap ELAN 4 Fixed Duraguard Recalled for Mislabeling (1 Unit, 2025)

Aesculap AG is recalling one unit of the ELAN 4 Fixed Duraguard Standard, model GB942R, distributed in the United States to Missouri and internationally to multiple countries. The recall addresses mislabeling where the Standard was labeled as Long and the Long was labeled as Standard. Patients and healthcare providers should stop using this device immediately and follow the manufacturer’s recall指南

Aesculap AG
Mislabeling. The
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Health & Personal Care
HIGH
FDA DEVICE

CorNeat Vision EverPatch Recalled for Conjunctival Wound Dehiscence Risk (630 Units, 2025)

CorNeat Vision recalled 630 EverPatch surgical matrices distributed worldwide, including in 28 U.S. states. Review of complaints found conjunctival wound dehiscence may lead to early exposure of the patch. Stop using the device immediately and follow the manufacturer’s recall instructions. Contact CORNEAT VISION, LTD. or your healthcare provider for guidance.

CorNeat Vision
Reviewed complaints
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Health & Personal Care
HIGH
FDA DEVICE

Aesculap AG Recalls ELAN 4 Fixed Duraguard Long Mislabeling Devices (GB943R)

Aesculap AG recalls the ELAN 4 Fixed Duraguard Long device, Model GB943R, after mislabeling errors were discovered. The U.S. distribution reached Missouri with international distribution to multiple countries. Healthcare providers should stop using the device immediately per manufacturer instructions.

Aesculap AG
Mislabeling. The
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Health & Personal Care
HIGH
FDA DEVICE

Corneat Vision EverPatch+ 180-Unit Recall for Scleral Patch Dehiscence Risk (2025)

CORNEAT VISION recalled 180 units of EverPatch+ scleral reinforcement patch worldwide after complaints of conjunctival wound dehiscence. The issue can lead to early exposure of the surgical patch. Clinicians and patients should stop using the device immediately and follow the manufacturer recall instructions.

CORNEAT VISION
Reviewed complaints
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Food & Beverages
HIGH
FDA FOOD

Tampa Maid Foods Frozen Shrimp Recalled for Cs-137 Contamination (2025)

Tampa Maid Foods recalled 776 cases of Panko Style Breaded Butterfly Shrimp due to potential Cesium-137 contamination. The product was distributed to 16 states. Consumers should not eat the shrimp and should contact the company for refunds or replacements.

TAMPA MAID FOODS
Product may
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Food & Beverages
HIGH
FDA FOOD

ADMIRAL OF THE FLEET, PORTICO SEAFOOD CLASSIC Breaded Shrimp Recalled Over Cs-137 Contamination (120

ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC Cleantail Breaded Butterfly Shrimp is recalled by TAMPA MAID FOODS, LLC after the FDA identified Cesium-137 contamination. The recall covers 1,200 cases distributed to multiple states. Consumers should not consume the product and should contact TAMPA MAID FOODS for refund or replacement.

ADMIRAL OF THE FLEET
Product may
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe 61,334 Reverse Shoulder Humeral Liners Recalled Worldwide (2025)

Exactech recalled 61,334 Equinoxe reverse shoulder humeral liners sold worldwide after finding the articular surface position outside labeling dimensions. The recall covers REF 320-38-00, REF 320-38-03, REF 320-42-00, and REF 320-42-03. Healthcare providers and patients should stop using the devices immediately and follow recall instructions distributed by email.

Exactech
Reverse Shoulder
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe Recalled 11,542 HumeraL Liners Worldwide Over Dimension Mismatch (2025)

Exactech recalled 11,542 Equinoxe reverse shoulder humeral liners worldwide after finding the articular surface position outside labeling specifications. The recall covers several REF numbers and UDIs and is active as of 2025. Healthcare providers were advised to stop using affected liners and follow manufacturer instructions.

Exactech
Reverse Shoulder
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Health & Personal Care
HIGH
FDA DEVICE

Ethicon Stratafix PDS Plus Recall 516 Units for Barb Non-Engagement (2025)

Ethicon recalled 516 STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Devices sold worldwide through healthcare providers, including 18 U.S. states and Singapore and Malaysia. The defect is potential barb non-engagement that could compromise tissue control. Clinicians and patients should stop using the device immediately and follow recall instructions from Ethicon.

Ethicon
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Recalls Heartstring III Proximal Seal System 3.8 mm Occluder (32,867 Units) 0

Maquet Cardiovascular recalls the Heartstring III Proximal Seal System, a 3.8 mm intravascular anastomosis occluder used by hospitals worldwide. Three failure modes have been identified: loading failure, deployment failure, and failure to provide adequate hemostasis. Healthcare facilities should stop using the device immediately and follow manufacturer recall instructions.

Maquet Cardiovascular
Three failure
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Heartstring III Proximal Seal System Recalled for 168 Units Worldwide (2025)

Maquet Cardiovascular recalled 168 Heartstring III Proximal Seal System intravascular occluders worldwide, including the United States. Three failure modes have been identified: loading the Heartstring Seal, deploying it into the aortotomy, and achieving adequate hemostasis. Healthcare facilities should stop using the device and follow the manufacturer’s recall instructions.

Maquet Cardiovascular
Three failure
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Food & Beverages
HIGH
FDA FOOD

Anderson Candy Company Recalls 960,000 Peanut Rounds for Undeclared Soy Allergen (2025)

Anderson Candy Company recalled 960,000 Peanut rounds after undeclared soy allergen was found. The sizes are 2.25 oz and 3 oz. The affected distribution covers Oklahoma, Louisiana, Texas, Arkansas, Kansas, Missouri, Arizona, Alabama, Mississippi and Tennessee. Consumers should not eat the product and should contact the company for refund or replacement.

Anderson Candy Company
Undeclared soy
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Food & Beverages
HIGH
FDA FOOD

Great Value and Sea Best Raw Frozen Shrimp Recalled for Cs-137 Contamination (33,164 Lbs) 2025

Beaver Street Fisheries is recalling 33,164 pounds of Great Value and Sea Best raw frozen shrimp distributed to Arkansas, Florida and Illinois after Cs-137 contamination was detected. The product may be contaminated with Cesium-137, a radiological hazard. Consumers should not consume it and should contact Beaver Street Fisheries for refund or replacement.

Great Value
Product may
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Health & Personal Care
HIGH
FDA DEVICE

Mindray BeneVision N1 Patient Monitor Recall Issued for 2,278 Units Worldwide (2025)

Mindray DS USA, Inc. dba Mindray North America recalled 2,278 BeneVision N1 patient monitors distributed worldwide, including Canada. The devices may activate an abnormal alarm pause. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions issued by Mindray.

Mindray
Potential for
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Food & Beverages
HIGH
FDA FOOD

Stanley Pearlman Enterprises Recalls Whiting Fillet Over Date Error

Stanley Pearlman Enterprises recalled 141 cases of whiting fillets on August 15, 2025. The bags contain an incorrect best by date that misrepresents the product's shelf life. The fillets are actually good until January 11, 2027.

Stanley Pearlman Enterprises
Recall initiated
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Recalled Drinkmate 1L Carbonation Bottles
MEDIUM
CPSC

Drinkmate Recalls 1-Liter Carbonation Bottles for Explosion Risk

Drinkmate recalled certain 1-liter carbonation bottles after receiving reports of potential explosions. Users may suffer serious laceration and hearing damage from exploding bottles. Consumers should stop using the bottles immediately and contact Drinkmate for a free replacement.

Drinkmate
The recalled
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