Undeclared milk
All Recalls
95,114 total recalls in our database
Undeclared Milk. During an FDA investigation the manufacturer was notified that the label does not list the allergen milk in the ingredient statement.
The firm was notified after laboratory analysis that the product test positive for Listeria monocytogenes.
Cal Yee's Cajun Sesame Hot Sticks (1-lb plastic bag)
Cal Yee Farm
Undeclared wheat, Undeclared soybean oil
Cal Yee Farms Fruit Basket (50-oz)
Cal Yee Farm
Undeclared almonds
Cal Yee's Tropical Trail Mix - assorted nuts and dried fruits (8-oz, 1-lb, 2-lb, 5-lb plastic bags)
Cal Yee Farm
Undeclared milk
Cal Yee's New Orleans Hot Mix (1-lb plastic bag)
Cal Yee Farm
Undeclared wheat, Undeclared soybean oil
Underprocessing
Cal Yee's Dark Chocolate Almonds (8-oz plastic bag)
Cal Yee Farm
Undeclared milk
Kissable Diabetics Foot Cream, NET WT 4 oz (113 g) per tube, Manufactured By: Brands International Corp., Newmarket, ON, L3X 2S2. UPC 6 72008 80925 3
Brands International
CGMP Deviations: lack of adequate release testing.
CGMP Deviations; product intended for quarantine was inadvertently distributed
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Lack of 510(k) clearance.
Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation.
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
BD Pyxis Med ES Auxiliary (AUX), REF 343
CareFusion 303
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
Lack of 510(k) clearance.
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
Potential for hole in package compromising sterility of the medical kit.