Great Value Cherry Mixed Fruit, 4 oz, 4 Count and 12 count plastic cups sealed with clear film.
Walmart
FD&C Red No 3 was not declared as an ingredient.
92,900 total recalls in our database
Walmart
FD&C Red No 3 was not declared as an ingredient.
Tropical Nut & Fruit Company
Undeclared Almonds & Cashews. The firm was notified by their customers that the product contains a trail mix instead of the cheese mix. The trail mix contains almonds and cashews that are not listed in the ingredient statement.
Soybean Sauce is declared but Wheat is not declared.
Mayonnaise is declared but Soybean Oil and Egg are not declared.
Today's Frozen Desserts
Undeclared Yellow 5 & Yellow 6
Yucatan Products
Non-English labeling
Soybean Sauce is declared but Wheat and Fish (Anchovy) are not declared.
Zhejiang Jingwei Pharmaceutical Co.
Incorrect/Undeclared Excipients: The inactive ingredients labeled on the product boxes and tubes are listed as "mineral oil , petrolatum ". The inactive ingredients in the actual product are polyethylene glycol 400 , polyethylene glycol 4000.
Microbial Contamination of a Non-sterile Product: The product was found to be contaminated with Cohnella bacteria.
Failed Impurities/Degradation Specifications.
VIONA PHARMACEUTICALS
Crystallization
Breckenridge Pharmaceutical
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
LEICA BIOSYSTEMS NUSSLOCH GMBH
As part of our post market surveillance, we recognized that some customers are using flammable freezing sprays within the cryostat chamber. All flammable freezing sprays can potentially ignite and therefore can cause serious injuries. The flammability is indicated on the labelling of these sprays. The cryostat labelling, however, did not include any specific warning about usage of flammable freezing sprays prior to 2019.
MEDLINE INDUSTRIES, LP - Northfield
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
DATEX--OHMEDA
GE HealthCare has become aware that for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices, the screw that secures the doors that cover the warmer heaters may not have been torqued to specification. This may lead to the doors becoming loose.
Olympus Corporation of the Americas
Certain serial numbers of the CV-190 do not start up properly because parts that deviated from the specification were assembled into the power supply unit.
Merit Medical Systems
Inflation devices may have a small hole in the sterile barrier of the device and use of affected devices may result in exposure to pathogens/pyrogens which could lead to infection.
Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.
MEDLINE INDUSTRIES, LP - Northfield
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
MEDLINE INDUSTRIES, LP - Northfield
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.