95,075 total recalls in our database
The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.
The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.
Cardinal Health 200
The suction valve may not close properly which could cause continuous suction.
The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.
The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.
The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.
The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.
COVIDIEN MEDTRONIC
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal contents.
Unknown Manufacturer
The patches on the shorts can detach, posing a choking hazard to young children.
Fujian Anxi Shangqing Huaxing Handicraft Co. Ltd., of China
The chair's frame can break, posing a fall hazard to consumers.
Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm received a small number of customer complaints that reported an off-taste and off-odor of the product.
During a FDA foreign inspection, it was found that four products did not declare allergens.
Earthrise Nutritionals
The product may contain small metal pieces (approximately 2 mm to 8 mm) from a sifter screen.
Pinnacle Food Group
The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.
During a FDA foreign inspection, it was found that four products did not declare allergens.
Blue Bell Creameries, L.P.
Vanilla ice cream not labeled for individual sale was distributed to stores for individual sale. They are therefore missing a nutrition facts panel, an ingredients statement , and they do not declare the presence of the major food allergen milk
Del Monte Fresh Produce N.A., Inc. HQ
Del Monte has recalled the products because they may be linked to this recent cluster of illnesses and have the potential to be contaminated with Cyclospora
Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
During a FDA foreign inspection, it was found that four products did not declare allergens.
Peanut Processors
The firm was notified by their customer that the product test positive for Salmonella