Wilton Autumn Assorted Treat Toppings Sprinkles, 2.6oz (74g) 3 hanging clear plastic bags with 1 paperboard card, SKU 710-9722 UPC 070896097224
Wilton Industries
Undeclared milk
95,025 total recalls in our database
Wilton Industries
Undeclared milk
J & J Distributing Company
Products may be contaminated with Listeria monocytogenes.
The Buttermik powder may contain a Foreign Material (metal).
Metal fragment. The small thin metal piece is around 0.5 inch long without sharp edges, was found inside chocolate bar.
J & J Distributing Company
Products may be contaminated with Listeria monocytogenes.
Grace Kennedy Foods USA
Presence of plastic in bagged frozen peppers and onions.
Salmonella
Queso Cheese dip may contain foreign material (metal).
Wilton Industries
Undeclared milk
Wilton Industries
Undeclared milk
Temperature Abuse
Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
Crystallization: customer complaints for crystallization in finished product.
Crystallization: customer complaints for crystallization in finished product.
Nuvasive Specialized Orthopedics
Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.
It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.
A small percentage of implanted cardiac devices, from a well-defined subset, may experience a shortened Recommended Replacement Time (RRT) to End of Service (EOS) interval following an earlier-than-expected RRT observation
Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+) Tibial Bases due to potential damaged packaging. These implant components are utilized in Total Knee Arthroplasty. The affected tibial bases are designed to be used in cemented applications.
It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.