Hi Tech Pharmaceuticals ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY recall — FDA F-0501-2021
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
Track recent U.S. food recall enforcement reports from the FDA. Review recalled products, reasons, classifications, recalling firms, distribution details and official record identifiers when available.
16,552 detailed records are currently available in this category.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
Inspection by California Department of Public Health found that labeling did not properly declare milk.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
The firm was notified by an ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that…
Incorrect active ingredient is listed on product label
The firm was notified by its ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that…
Firm determined that pesticide Bifenazate MRL is out of compliance for the US market. US MRL = 5ppm. Product tested = 5.8ppm.
Notified by packaging supplier of recall due to potential loose particles of CPET in product packaging that could become imbedded in the finished baked goods.
The Hershey Company, 19 East Chocolate Avenue, Hershey PA 17033 is voluntarily recalling of a specific lot of Hershey s Chocolate Shell Topping in a 7.25-oz. (205g) bottle UPC (346000)…
Ingredients statement declares Unsalted Cream but does not list milk. Label has allergen advisory statement "Mfg on same equipment that processes wheat, egg, peanut & tree nut. May contain…
Michigan Department of Agriculture and Rural Development sampled Enoki mushrooms and found some samples to be positive for Listeria monocytogenes.
One lot of ALA 300 mg Cap-50 were labeled at Melatonin 3 mg Tab-60.
Bueno Coffee Substitute Pecan Praline Gluten-Free product contains undeclared peanut and barley (which contains gluten).
Products have the potential to be contaminated with Salmonella. The cashew cheese is suspect in a current outbreak.
Failure to manufacture product in accordance with 21CFR part 114: Acidified Foods
Products have the potential to be contaminated with Salmonella. The cashew cheese is suspect in a current outbreak.
Products have the potential to be contaminated with Salmonella. The cashew cheese is suspect in a current outbreak.
SnoBalls snack cakes were packaged with a label for Chocolate CupCakes causing the product to fail to declare the major food allergen coconut.
Bueno Coffee Substitute Creamy Hazelnut product contains undeclared hazelnut and peanut.
Products have the potential to be contaminated with Salmonella. The cashew cheese is suspect in a current outbreak.
Products have the potential to be contaminated with Salmonella. The cashew cheese is suspect in a current outbreak.
Product potentially contains undeclared almonds.
Dark Chocolate walnuts were packed in a container labeled at Dark Chocolate Espresso Beans and does not declare walnuts as an allergen Bottom label with nutritional information is correct…
FDA enforcement reports are classified by potential health hazard. Class I is the most serious classification, while Class II and Class III generally indicate lower levels of risk. The classification shown here comes from the official FDA record.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.