95,114 total recalls in our database
Polaris Industries Inc., of Medina, Minnesota
The improperly routed brake line can contact the front wheels during vehicle operation resulting in brake line damage and brake loss, posing a crash hazard.
Unknown Manufacturer
The small plastic piece containing a high-powered magnet that connects one train to another can detach or become loose, posing choking and magnet ingestion hazards.
Dick Taylor
Undeclared allergen (peanut)
Maisie Jane's California Sunshine Products
High levels of aflatoxin
The Little Oak Company
No pre-market notification and Mixing instructions not in ounces
Unapproved food additive.
Fairfield Gourmet Food Corp d/b/a David's Cookies
Fairfield Gourmet Food Corp. d/b/a David s Cookies ,28 Industrial Road, Fairfield NJ 07004has initiated a recall of Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g) plastic package (i.e.) Clamp shell 8 package per case, LOT # BS23212 (Manufactured on July, 31, 2023) because of MISLABELED / UNDECLARED ALLERGENS (Peanuts)
The Little Oak Company
No pre-market notification and Mixing instructions not in ounces
Comercializadora Pepsico Mexico,
Undeclared Allergen: Soy
Undeclared allergen (egg)
Cross Contamination with Other Products: Potential cross-contamination of ibrexafungerp citrate drug substance with ezetimibe (a non-antibacterial beta-lactam compound).
Cardinal Health 200
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
TECHNO-PATH MANUFACTURING
Technopath Manufacturing Ltd. has identified an issue with the glass vial commodity used to fill the Multichem S Plus Level 1, Multichem S Plus Level 2, Multichem S Plus Level 3, Multichem IA Plus and Multichem P Controls. Some customers have experienced broken vials when receiving or thawing Technopath Multichem IA Plus and Multichem S Plus Controls. Breakages have been observed upon delivery, while thawing or while opening the vial. The breakages can result in the bottom of the vial breaking off, breakage in the neck thread area or cracking on the sides of the vial. This may expose the user to biohazardous material if cut and may cause a delay in patient results.
Mazor Robotics
Software update
Cardinal Health 200
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Fresenius Medical Care Holdings
Potential PCBA leaching from tubing of hemodialysis machines.
Encore Medical
Reverse shoulder prosthesis package that should contain 5mmx30 screws could contain incorrect 3.5mmx30 screws. Use of incorrect screws could result in surgical delay and inadequate fixation.
Alcon Research
Ophthalmic microsurgical vision systems have a new Printed Circuit Board (PCB) design that could lead to higher voltage to a PCB component, that could cause component failure and loss of pressure control for the use of cutters, scissors, and forceps, which could lead to an increased risk of microbial infection, tissue damage and progressive visual impairment.
Fresenius Medical Care Holdings
Potential PCBA leaching from tubing of hemodialysis machines.
RoyalVibe Health
Ultrasound devices were not authorized, cleared, or approved by FDA, and thus their performance characteristics have not been adequately established. There is a possibility of customers' reliance on marketing claims which could cause the user to forgo medical treatment resulting in health consequences.