Treehouse Foods DUNCAN HINES 1/3.12kg GRDL WFL BLGN ORIG 4IN - DUNHN UPC recall — FDA F-0179-2025
potential to be contaminated with Listeria monocytogenes
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
potential to be contaminated with Listeria monocytogenes
potential to be contaminated with Listeria monocytogenes
potential to be contaminated with Listeria monocytogenes
potential to be contaminated with Listeria monocytogenes
potential to be contaminated with Listeria monocytogenes
potential to be contaminated with Listeria monocytogenes
potential to be contaminated with Listeria monocytogenes
CGMP violations.
cGMP Deviations
CGMP violations.
cGMP Deviations
Tesla, Inc. (Tesla) is recalling certain 2024 Model X vehicles. The parking lights and low beam headlights may flicker. As such, these vehicles fail to comply with the requirements of…
Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs Stress-B-Plus Dietary Supplement Tablets, 90 tablets per bottle. The bottle is white and made of plastic. Lot…
Undeclared egg
Product contains undeclared sulfites. The product was sampled by the NYSAGM s Food Safety Division and tested positive at 120.7 PPM Sulfites.
Undeclared egg
potential to be contaminated with Listeria monocytogenes
Undeclared egg
Undeclared egg
Chrysler (FCA US, LLC) is recalling certain 2022-2024 Jeep Grand Cherokee and 2021-2024 Jeep Grand Cherokee L vehicles. An improperly secured connector for the front seat side air bags…
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles. The fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet.
Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Browse recent months with enough recall history for useful comparison.