125 recalls tagged with “laceration risk”.
Luyuan recalled X-Pro Eagle 40cc and FRP Sahara 40cc Youth ATVs on December 11, 2025. The ATVs violate mandatory safety standards and pose serious injury risks. Consumers must stop using the ATVs and contact Luyuan for a free repair.
Primark recalls the Little Bear 2-pack Soother Clips due to hazards. The recall affects all units sold from June to August 2025. Consumers should stop using them immediately and return for a refund.
Intuitive Surgical recalled 86,904 da Vinci S and Si Monopolar Curved Scissors instruments sold worldwide to hospitals and surgical centers. The recall cites increased complaints of broken or frayed grip cables on reusable instruments. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.
Intuitive Surgical recalled 2,095 units of the da Vinci S, Si EndoWrist Tenaculum Forceps Instrument distributed nationwide in the United States and in multiple countries after reports of frayed or broken pitch cables. The defect can compromise instrument control during surgery. Hospitals and surgeons should stop using the device immediately and follow recall instructions from Intuitive Surgical.
Intuitive Surgical recalled 6,152 da Vinci S, Si Permanent Cautery Hook Instruments distributed to U.S. hospitals and clinics overseas. The defect involves frayed or broken pitch cables. Healthcare facilities should stop using the instruments immediately and follow manufacturer recall instructions. If you operate with these tools, consult your supplier or Intuitive Surgical for next steps.
Intuitive Surgical recalled 7,819 units of the da Vinci S/Si Mega Needle Driver Instrument sold worldwide to hospitals and healthcare providers. The recall cites broken or frayed grip cables that can impair instrument control. Stop using the device and follow the manufacturer’s recall instructions for replacement or service.
Intuitive Surgical recalled 2,370 units of the da Vinci S, Si Double Fenestrated Grasper Instrument distributed worldwide on December 9, 2025. The EndoWrist instruments use mechanical cables to transmit motion. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.
Ningbo Tianqi Electronic recalled FUFU&GAGA Murphy wall beds on December 4, 2025. The 215-pound frame can fall, posing impact and laceration hazards. Consumers should stop using the beds and seek refunds immediately.
Grizzly Industrial recalled all 15" 3HP heavy-duty planers with model number G0815 on December 4, 2025. The planers pose impact and laceration hazards due to a defect that allows the chip breaker to contact the cutterhead blades. Consumers should stop using the planers immediately and contact Grizzly for a free repair kit.
Nate's Fine Foods recalled 972 cases of cooked linguine pasta on September 25, 2025. The recall follows potential contamination with Listeria monocytogenes. Consumers in CA, IN, PA, and TX should not consume the product.
Wegmans Food Markets recalled 2,773.9 pounds of grated cheese on November 22, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not consume the product and seek refunds immediately.
GBC Food Services recalled 11 units of EverRoast Chicken Caesar Wrap on November 22, 2025. The recall occurred due to potential contamination with Listeria monocytogenes. The affected products were distributed in Kentucky and Indiana.
GBC Food Services recalled EverRoast Chicken Caesar Salad on November 22, 2025, due to potential Listeria monocytogenes contamination. The recall affects 2 units of the product distributed in Kentucky and Indiana. Consumers should not consume this product and seek a refund or replacement.
Ambriola Co., Inc. recalled 1,015 bags of Sam's Pecorino Romano grated cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a harmful bacteria. Consumers should not consume the product and seek a refund or replacement immediately.
Boar's Head recalled 2,106 units of Grated Pecorino Romano on November 21, 2025. The product tested positive for Listeria Monocytogenes, a harmful bacterium. Consumers should avoid consumption and seek refunds or replacements.
Ambriola Co., Inc. recalled 6,632 units of Grated Pecorino Romano cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a dangerous bacteria that can cause serious illness. Consumers should not consume the affected product and should seek refunds or replacements.
Ambriola Co., Inc. recalled 179 bags of grated Pecorino Romano on November 21, 2025. The product tested positive for Listeria Monocytogenes, prompting immediate consumer action. It was distributed across 15 states, including California and Texas.
Ambriola Co., Inc. recalled 45 bags of Pinna Grated Pecorino Romano on November 21, 2025, after Listeria Monocytogenes was detected. The recall affects products distributed in 17 states including California and Texas. Consumers should not consume the recalled product and should seek refunds or replacements.
Ambriola Co., Inc. recalled 184 units of Grated Pecorino Romano cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a harmful bacteria that can cause serious illness. Consumers in multiple states should not consume this product.
Ambriola Co., Inc. recalled 964 bags of Grated Pecorino Romano on November 21, 2025. The product tested positive for Listeria Monocytogenes, a serious health threat. Affected states include AZ, CA, CO, and more.