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.
2,775 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Aesculap AG recalled three surgical instruments on August 18, 2025, due to mislabeling issues. The ELAN 4 FIXED DURAGUARD LONG was incorrectly labeled as "Standard" and vice versa. The recall affects devices distributed in the U.S. and several international markets.
Aesculap AG recalled one unit of the ELAN 4 FIXED DURAGUARD STANDARD on August 18, 2025. The product was mislabeled, leading to potential use confusion. The recall affects distribution in the US and multiple international locations.
CorNeat Vision recalled 630 units of the EverPatch surgical matrix on August 18, 2025. The recall follows complaints of conjunctival wound dehiscence leading to potential exposure of the surgical patch. The product was distributed worldwide, including across numerous U.S. states.
CORNEAT VISION recalled 180 units of EverPatch+ on August 18, 2025, due to a risk of conjunctival wound dehiscence. This defect may lead to early exposure of the surgical patch. The recall affects distribution across the United States and several countries.
Tampa Maid Foods recalled 776 cases of Panko Style Breaded Butterfly Shrimp on August 16, 2025. The product may be contaminated with Cesium-137, a radioactive substance. Consumers should not eat the shrimp and should seek refunds or replacements.
TAMPA MAID FOODS recalled 1,200 cases of Cleantail Breaded Butterfly Shrimp on August 16, 2025. The product may contain dangerous levels of Cesium-137. Consumers should not eat this shrimp and seek a refund immediately.
TAMPA MAID FOODS recalled 31 cases of Breaded Butterfly Shrimp on August 16, 2025, due to potential contamination with Cesium-137. The product, sold in bulk packaging, may pose serious health risks. Consumers should not consume the shrimp and seek refunds immediately.
Anderson Candy Company recalled 960,000 units of Peanut Rounds on August 15, 2025. The recall stems from undeclared soy allergens that pose a serious health risk. The affected products were distributed in several states including Texas and Louisiana.
Maquet Cardiovascular recalled 32,867 units of the Heartstring III Proximal Seal System on August 15, 2025. Three failure modes can lead to inadequate hemostasis during procedures. Patients and healthcare providers must stop using this device immediately.
Exactech recalled 11,542 reverse shoulder humeral liners on August 15, 2025. The devices have an articular surface position outside of the specified dimensions. This recall affects units distributed worldwide, including several U.S. states.
Exactech recalled 61,334 units of Reverse Shoulder Humeral Liners on August 15, 2025. The liners do not meet specified dimensional standards, posing a risk to patients. Healthcare providers and patients must stop using the devices immediately.
Maquet Cardiovascular recalled 16,512 Heartstring III Proximal Seal Systems due to critical failure modes. The recall affects devices distributed globally since August 15, 2025. Users must stop using the device immediately and follow manufacturer instructions.
ETHICON recalled 516 units of the STRATAFIX Spiral PDS Plus device on August 15, 2025. The recall follows reports of potential barb non-engagement that could affect surgical procedures. Healthcare providers and patients must stop using the device immediately.
Mindray DS USA, Inc. recalled 2,278 BeneVision N1 Patient Monitors on August 15, 2025. The monitors may activate an abnormal alarm pause, compromising patient safety. Health professionals must cease using these devices immediately and follow recall instructions.
Beaver Street Fisheries recalled 33,164 pounds of Great Value and Sea Best raw frozen shrimp on August 15, 2025. The product may contain Cesium-137, a radioactive substance. Consumers should not consume the affected shrimp and should seek refunds.
Maquet Cardiovascular recalled the Heartstring III Proximal Seal System on August 15, 2025, due to three identified failure modes. These failures include issues with the seal's loading, deployment, and hemostasis. The recall affects 168 units distributed worldwide.
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.
Firefly Fuel recalled 32 oz. Safe & Green fuel bottles on August 14, 2025. The bottles pose a serious poisoning risk to young children due to non-compliant packaging. Consumers should stop using the product immediately and contact Firefly for a replacement lid.
Empower Brands recalled Remington hair dryers on August 14, 2025, due to electrocution risks. The D3190DCDN model lacks immersion protection, posing a danger if dropped in water. Consumers should stop using the product immediately.
ESR recalled HaloLock wireless power banks on August 14, 2025, following reports of fire hazards. The lithium-ion batteries can overheat and ignite. Consumers should stop using these devices immediately and return them for a full refund.