XinXing Dried Plum, Net Wt. 5.3 oz.(150g)
Rong Shing Trading NY
Product contains dried peaches, but front labeling of product stated dried plums
95,114 total recalls in our database
Rong Shing Trading NY
Product contains dried peaches, but front labeling of product stated dried plums
FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.
May contain undeclared milk
Freedman Food Service, Inc
Product may contain undeclared Milk (whey listed in ingredients)
Ocean Spray Cranberries
Product contains undeclared sulfites.
Dark Chocolate mint bar contains undeclared milk
Alfa Vitamins Laboratories
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
Freedman Food Service, Inc
Product may contain undeclared Wheat, Soy, Eggs, and Milk
Homestead Creamery
Unsalted butter has potential to be contaminated with Listeria monocytogenes.
Amneal Pharmaceuticals of New York
CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.
Failed Stability Specifications: Out-of-Specification (OOS) results for High Molecular Weight Polymers.
Dr. Reddy's Laboratories
Discoloration: product contains brown pellets
Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment.
To reinforce existing instructions within the Directions for Use (DFU) and provide further guidance which will be added to the DFU that may reduce the likelihood of metal cap and fiber tip break temperature related complaints.
Philips North America
When a user acquires XperCT scan on an Azurion 2.0 system, enters the XperGuide guidance step and moves the L-arm away from the initial scan position before starting the live guidance, a warning message directs the user to move the L-arm stand back to the initial XperCT scan position. Although the software generates this message, it does not prevent the use of live guidance if the L-arm stand is not repositioned. Using live guidance with a mispositioned L-arm can result in the display of an incorrect overlay and needle path.
Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment.
Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment.
Baxter Healthcare
Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
Potential issue with the manufacture and inspection of U-channel sheaths in Implantation Instruments Sets. Affected U-channel sheaths may be more likely to cause damage to ProACT implant devices when passes through the sheaths.
GE Healthcare
An issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.