Progressive Laboratories recalled four dietary supplement products including Testosterzone, Thyroid Resilience, and Xenesta Nuvive formulations due to undeclared milk. Consumers with milk allergies who take these supplements risk an allergic reaction.
Class I — A reasonable probability that eating this product will cause serious health problems or death.
Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap; Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap; Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap; Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Recalled dietary supplements may contain undeclared milk.
| Recall # | Product | Lot / code | Status |
|---|---|---|---|
| F-0912-2018 | Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap | Lot # 2072237 | Terminated |
| F-0913-2018 | Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap | Lot # 2114667 and 2061167 | Terminated |
| F-0914-2018 | Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap | Lot # 2071887 | Terminated |
| F-0915-2018 | Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap | Lot # 2071957 and 2082387 | Terminated |
Prime Line Distributors and Ferrarini USA recalled imported ready-to-eat pork guanciale products due to possible Listeria contamination. Consuming contaminated product could cause serious infection, particularly in vulnerable populations.
Made Fresh Salads recalled ready-to-eat deli style salads and cream cheese due to potential Listeria monocytogenes contamination. Listeria infection can cause severe illness and is particularly dangerous for pregnant women, young children, and immunocompromised individuals.
Foods Alive Inc. recalled Foods Alive Moringa Leaf Powder due to potential Salmonella contamination. Consumers who have this product should not use it, as Salmonella can cause serious foodborne illness.
American Regent recalled Epinephrine Injection USP 30 mg/30 mL multi-dose vials due to potential particulate matter and loss of sterility assurance. Users of affected vials face serious risk if the contamination is present, as injection of particles or non-sterile product could cause infection or other harm.
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