Cranberry Sweets & More Recalled Meltaways product is packaged in clear cellophane recall — FDA F-0214-2023
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Complete FDA and NHTSA recall records dated in 2023, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Potential contamination of plastic particles.
Sunrise Logistics Inc/ Four Seasons Produce Inc, 400 Wabash , Road Ephrata, PA 17522 has initiated a recall of, PROPAL Hass Avocados, Bag of 6 pieces, Green net with green plastic film, 11…
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Lack of assurance of sterility: Bags have the potential to leak.
Volvo Car USA, LLC (Volvo Car) is recalling certain 2019-2022 V60CC, XC60, and XC90 vehicles. During steering gear assembly, double screws may have been assembled on top of each other,…
Distribution without Pre-Market Clearance
Distribution without Pre-Market Clearance
Distribution without Pre-Market Clearance
Distribution without Pre-Market Clearance
Undeclared collagen (bovine dermis) casing
Product found to contain wheat that is not declared on the label.
Product contains undeclared sulfites (17.9mg/serving).
Undeclared collagen (bovine dermis) casing
No label on packaged product
Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.
Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.
CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.