Philips Ingenia 1.5T S, Magnetic Resonance System recall — FDA Z-1565-2024
Patient support table floor plate may be incorrectly installed.
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.
Patient support table floor plate may be incorrectly installed.
Salmonella contamination
Product recalled due to the presence of yellow oleander and its components in the product.
Undeclared allergen milk (whey) and undeclared lard
Product recalled due to the presence of yellow oleander and its components in the product.
Foreign material (metal) in donuts
Sea Salt Almond Allegator candy has a back label for chocolate covered cherries.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Foreign material (metal) in donuts
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product has been recalled because it may exceed FDA guidance levels for leachable lead.
Coconut is declared in the ingredient list, but not declared in the contains statement in coconut paste.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
May contain foreign material (plastic)
Foreign material (metal) in donuts
Product recalled due to the presence of yellow oleander and its components in the product.
Superpotent Drug: Due to overfilling of drug powder
Kia America, Inc. (Kia) is recalling certain 2024 Sorento vehicles. The motor driven power steering (MDPS) wiring harness may be incorrectly assembled, which can result in a loss of power…
Browse recent months with enough recall history for useful comparison.