Minnesota recalls

Undeclared allergen: milk

Product Contamination

Potential Listeria monocytogenes contamination

Potential Listeria monocytogenes contamination

Potential Listeria monocytogenes contamination

Undeclared allergen:Wheat

Sprouts may be contaminated with Listeria monocytogenes.

Sprouts may be contaminated with Listeria monocytogenes.

Undeclared Fish Allergen

Incomplete pasteurization

Incomplete pasteurization

Incomplete pasteurization

Incomplete pasteurization

Incomplete pasteurization

Milk may contain undeclared almond from almond milk

Import Violation

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.

Product was recalled due to the potential for contamination with Salmonella

Potential mold contamination.

Product is labeled as electrolytes but is actually caffeine

FD&C Red No 3 was not declared as an ingredient.

FD&C Red No 3 was not declared as an ingredient.

Possible Fragmentation of Ice Cream Tub (Container) Made of Compostable Material.

Insulin pumps that have been dropped, bumped, or experienced physical impact may have damage to internal electrical components, which may cause reduced pump battery life. Since the defect reduces the battery life overall, it shortens the time between low battery alarms and increases the frequency with which the user must insert a new battery. Further, the defect may also deliver the low battery alarm when there is significantly less time before the battery completely runs out, from the expected up to 10-hour buffer the low alert is supposed to signal, leading to device powering down and stopping insulin delivery unexpectedly. Per the firm, a subset of pumps with the defect showed the low alert alarm was delivered ~2.5 hours before the device shut off, however, patient reports indicate the time could be even shorter. Replacing the battery will not resolve this issue and the short battery life and the truncated low battery alert lead time will continue to occur. Early battery depletion could result in power loss and insulin delivery could be interrupted, resulting in under delivery of insulin potentially leading to hyperglycemia and/or DKA.

Insulin pumps that have been dropped, bumped, or experienced physical impact may have damage to internal electrical components, which may cause reduced pump battery life. Since the defect reduces the battery life overall, it shortens the time between low battery alarms and increases the frequency with which the user must insert a new battery. Further, the defect may also deliver the low battery alarm when there is significantly less time before the battery completely runs out, from the expected up to 10-hour buffer the low alert is supposed to signal, leading to device powering down and stopping insulin delivery unexpectedly. Per the firm, a subset of pumps with the defect showed the low alert alarm was delivered ~2.5 hours before the device shut off, however, patient reports indicate the time could be even shorter. Replacing the battery will not resolve this issue and the short battery life and the truncated low battery alert lead time will continue to occur. Early battery depletion could result in power loss and insulin delivery could be interrupted, resulting in under delivery of insulin potentially leading to hyperglycemia and/or DKA.

Potential foreign material (metal)

Potential foreign material (metal)

Acidified product was manufactured by firm without ODA license.

Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400 mg tablet was found in a 1000-count bottle of Atorvastatin Calcium Tablets, USP 40 mg.

Product Contamination