raw, yellow onions (whole peeled), intended for food service, packaged into plastic bags (5-lbs)
Taylor Farms Colorado
🍎 Food Class I - Dangerous
Potential contamination of E. coli O157:H7
All Recalls
95,114 total recalls in our database
raw, yellow onions (whole unpeeled), intended for food service, repacked into in 5-lb plastic bags
Taylor Farms Colorado
🍎 Food Class I - Dangerous
Potential contamination of E. coli O157:H7
Potentially contaminated with E. coli O157:H7.
raw, yellow onions (sliced, diced, slivered, ringed), intended for food service, packaged in plastic bags
Taylor Farms Colorado
🍎 Food Class I - Dangerous
Potential contamination of E. coli O157:H7
Del Monte Fresh Produce, Pineapple and Apple Salad 4/6.5oz plastic container, four containers per case. Refrigerated. Lot Code 02277101, expiration date 10/10/2024 .
Del Monte Fresh Produce N.A.
🍎 Food Class I - Dangerous
The product is being recalled due to an undeclared allergen - tree nuts (walnuts).
Westby Pepper Cheese Curds, 12 oz. (340g) UPC 7 50388-30105 2. Keep Refrigerated. No Added Preservatives. Manufactured by Westby Cooperative Creamery, Westby, WI 54667.
Westby Cooperative Creamery
🍎 Food Class I - Dangerous
Cheese curds may be contaminated with generic E. coli.
raw, yellow onions (whole unpeeled), intended for food service, in 50-lb corrugated boxes
Taylor Farms Colorado
🍎 Food Class I - Dangerous
Potential contamination of E. coli O157:H7
Berkeley Springs Water Purified , Berkeley Springs Water Distilled , One Gallons & Five Gallons, Plastic, 6 gallons in one case and1 individual 5 Gallon, Codes 090326,090426,090526,090626.
Berkeley Club Beverages
🍎 Food Class I - Dangerous
Product tested positive for coliforms.
🍎 Food Class I - Dangerous
Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
154784 1 / 5LB IMPERIALFRESH PROC FAJITA GRN PEPRED PEP W All lot codes
FreshPoint Denver, Incorporated
🍎 Food Class I - Dangerous
Potentially contaminated with E. coli O157:H7.
Hydralazine HCl Tablets, USP, 25mg, Rx only, 100 tablets per carton, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, Distributed by: MAJOR Pharmaceuticals, Livonia, MI, 48152, USA, NDC 0904-6441-61.
The Harvard Drug Group LLC
💊 Drugs Class I - Dangerous
Failed Impurities/Degradation Specifications; during routine stability testing for impurities.
💊 Drugs Class I - Dangerous
Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.
💊 Drugs Class I - Dangerous
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac and phenylbutazone.
💊 Drugs Class I - Dangerous
Subpotent Drug
💊 Drugs Class I - Dangerous
Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.
🏥 Medical Devices Class I - Dangerous
Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
🏥 Medical Devices Class I - Dangerous
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
🏥 Medical Devices Class I - Dangerous
There is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
Boston Scientific POLARx BALLOON CATHETER LT 28MM OUS, Material Number M004CRBS2100
Boston Scientific
🏥 Medical Devices Class I - Dangerous
Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
🏥 Medical Devices Class I - Dangerous
There is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries