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.
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
Due to a software error, it was observed that when the user closes the access door, the system will resume its scan cycle automatically, instead of the user initiating x-ray generation from…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
Pre-procedural issues related to software defects
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the…
Software update to correct several issues that include (1)Potential data loss, (2) Study mix-up, (3) Incorrect measurements on multi-frame images, (4) Dearchiving issue, and (5)…
Products may contain undeclared soy lecithin.
Products have the potential to be contaminated with Listeria monocytogenes.
The firm received Ice Oatmeal Cookies that actually contain Coconut Macaroon Cookies. Product is being recalled due to mislabeling. Product contains both milk and tree nuts that are not…
A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.
Product is labeled as Tonkotsu, but the actual flavor packet inside is Assari Shoyu , which contains a fish (sardines).
Rapid Alert System for Food and Feed notification received from Italy regarding high histamine levels in imported anchovy sauce.
Products have the potential to be contaminated with Listeria monocytogenes.
Firm determined that their Rice Cake Soup has undeclared milk in the form of sodium caseinate.
Kvas, a fermented non-alcoholic drink, due to bulging. A hole was punched to the lids of the gallon plastic jugs to prevent the plastic jugs from bulging. The package integrity was…
Claudio Specialty Foods is recalling anchovy sauce after receiving a telephone call from their supplier notifying them that the product was found to contain high levels of histamine.
A consumer purchased who purchased a labeled Coat & Bake Chicken but actually contained Pork Seasoning. The Pork Seasoning product contains the major food allergen "Milk" not declared on…
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