Perouse Medical in France initiated a voluntary recall of certain batches of Perouse FLAMINGO Inflations Devices due to a potential water-tightness default. The potential default could cause an air entry when the plunger is positioned around 20 mL.
All Recalls
95,114 total recalls in our database
The Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius Plate System) were found to be labeled incorrectly. Part no. 03.111.600 (Right) was found in the package labeled part no. 03.111.601 (Left). The laser etching denoting the orientation on the part is correct.
CPB Catheter Kit Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior vena cava.
Terumo Cardiovascular Systems
During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications
The case label correctly states partial rebreather but the insert label incorrectly states non-rebreather.
The QLAB a2DQ and aCMQ features have a defect that may use incorrect measurement values under specific conditions.
During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications
During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications
The product can be difficult to remove from the Distal Stem both out of the package and after proximal reaming.
Sarns Soft-arc Aortic Cannula 8.0mm curved tip, suture flange, 3/8" flare Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.
Terumo Cardiovascular Systems
During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications
"Advocate Redi-Code + BMB-BA006A Blood Glucose test strips" are inappropriately labeled and marketed as "Advocate Redi-Code + Blood Glucose test strips".
During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications
Recreational off-highway vehicles
Unknown Manufacturer
The vehicle's floor boards can allow a stick or other debris to break through and protrude into the foot rest area, posing an injury hazard to the operator and front passenger.
Philips "Lightolier" brand AF4SY Decorative Glass Lens
Gray Glass Company, of Queens Village, NY
The decorative glass lens can shatter and result in falling pieces of glass, posing a risk of laceration to the consumer.
Glass Beverage Dispenser
Unknown Manufacturer
The metal stand supporting the glass dispenser can break, posing an injury hazard to consumers.
Tommee Tippeeยฎ Monitor with Movement Sensor Pad
Unknown Manufacturer
Child can pull sensor pad cord into crib and wrap around the neck, posing a strangulation hazard.
Metabo Ergo series 6-inch angle grinders
Metabo Corp., of West Chester, Pa.
The on/off switch can stick in the "On" position, posing a laceration hazard.
Eggs have the potential to be contaminated with Salmonella Enteritidis
Cream; Sold in bulk; No labeling
Pearl Valley Cheese
Milk used in the products tested positive for antibiotics
Nestle is recalling the Hยฟagen-Dazs Chocolate Chocolate Chip Ice Cream because it was mislabeled and the ingredient statement does not identify peanuts. The affected products are labeled as Hยฟagen-Dazs Chocolate Chocolate Chip Ice Cream, and the lids are labeled as Hยฟagen-Dazs Chocolate Peanut Butter. These mismatched packages contain Chocolate Peanut Butter ice cream, and the ingredient stateme
Undeclared milk found in bars labeled "dairy free" or "vegan."