Lake Wolf Creamery ribbon cheese, refrigerated, vacuum packaged in flexible recall — FDA F-0086-2022
The milk pasteurization temperature was not recorded and/or the air space temperature was not at 150F or above as required.
Complete FDA and NHTSA recall records dated in October 2021.
These records include useful source details for the selected month.
The milk pasteurization temperature was not recorded and/or the air space temperature was not at 150F or above as required.
A customer notified the firm that the product contained glass pieces.
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
A customer notified the firm that the product contained glass pieces.
A customer notified the firm that the product contained glass pieces.
Milk products and shipped without being properly pasteurized.
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Whole and sliced Apple and Cherry Pies from five stores in the Mid-Atlantic Region contain undeclared milk and egg.
Milk products and shipped without being properly pasteurized.
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Labeling: Label Lacks Warning or Rx Legend: Finished product did not include the statement on the flip cap vial, "WARNING: PARALYZING AGENT"
Failed Dissolution Specifications: results were above specification.
Out of specification result observed in a dissolution test at the 9-month long term stability time point.
Hyundai Motor America (Hyundai) is recalling certain 2021 Palisade vehicles. The brake fluid may be contaminated, which can cause the brake master cylinder inner-cup seals to swell, and…
Nissan North America, Inc. (Nissan) is recalling certain 2017-2019 Rogue Hybrid vehicles. Contact with the Electronic Control Module (ECM) bracket may damage the engine harness, causing a…
Tesla, Inc. (Tesla) is recalling certain 2020-2021, 2023 Model 3 vehicles. The left and/or right side curtain air bag may have been improperly secured to the roof rail, which could result…
Tesla, Inc. (Tesla) is recalling certain 2020-2021 Model Y and 2019-2021 Model 3 vehicles. The front suspension lateral link fasteners may loosen, allowing the lateral link to separate from…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.