Reser's Fine Foods FCF Item #404967, Costco Item #1506878, Cilantro Lime Crema recall — FDA F-1086-2024
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Complete FDA and NHTSA recall records dated in 2024, 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.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Product has the potential to be contaminated with Listeria monocytogenes.
Product has the potential to be contaminated with Listeria monocytogenes.
Foreign object; metal and plastic shavings.
Product has the potential to be contaminated with Listeria monocytogenes.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Elevated levels of lead found in product
Due to elevated levels of lead.
Product contains undeclared wheat.
Product has the potential to be contaminated with Listeria monocytogenes.
Undeclared wheat. Finished bakery product labels declared flour but did not specify wheat.
Product has the potential to be contaminated with Listeria monocytogenes.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Undeclared wheat. Finished bakery product labels declared flour but did not specify wheat.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Ford Motor Company (Ford) is recalling certain 2023 Maverick and Bronco Sport vehicles. The tires may have been manufactured incorrectly, which may result in a loss of vehicle handling and…
Subaru of America, Inc. (Subaru) is recalling certain 2020-2022 Outback and Legacy vehicles. A capacitor in the sensors for the Occupant Detection System (ODS) may crack and short circuit,…
Ford Motor Company (Ford) is recalling certain 2024 Mustang vehicles equipped with 2.3L engines. The low-pressure fuel supply line may be damaged or cut, which can result in a fuel leak.
Product failed sterility testing.
Three lots of the Boot Assembly, Traction Device are being recalled due to due to a customer report of an incorrectly oriented locking pin which caused the boot to detach from the traction…
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.