Twin City Foods Individually Quick Frozen recall — FDA F-1503-2023
Listeria monocytogenes
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.
Listeria monocytogenes
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Product appears to be Yellow Oleander instead of Nuez de la India as labeled.
Listeria monocytogenes
A piece of brittle plastic was found in seafood crabmeat stuffing mix.
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Listeria monocytogenes
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Foreign object; rocks.
Listeria monocytogenes
Listeria monocytogenes
Listeria monocytogenes
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Plastic foreign object found in product.
General Motors, LLC (GM) is recalling certain 2023 Cadillac Escalade, Escalade ESV, Chevrolet Suburban, Chevrolet Tahoe, GMC Yukon, and Yukon XL vehicles. The rear suspension outer control…
Lack of Assurance of Sterility: Powder discoloration due to small crack in some vials.
Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil, an ingredient found in a FDA approved product for the treatment of male sexual…
Chrysler (FCA US), LLC is recalling certain 2022-2023 Jeep Wrangler and Gladiator vehicles equipped with a manual transmission. The rearview camera may fail to display the rearview image…
Kia America, Inc. (Kia) is recalling certain 2019 Sorento vehicles. Due to a manufacturing error, water may leak into the rearview camera, which can cause the rearview camera image not to…
Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a portion of the visual field is obscured.
Sterility of device may be compromised due to breach of the chevron seal of the packaging
The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which exceeds the permissible exposure level calculated according to ISO 10993-17: 2002
Transducer, an ultrasound system accessory, consists of two parts that are bonded together that may come apart due to chassis bonding issue, which may pose risk to users and patients of…
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.