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.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
After a submission for CLIA database update from Focus Diagnostics to DiaSorin Molecular,the company found that their Legionella IFA device (IF0950) is not 510(k) exempt.
The system will completely stop allowing the downloading or acquisition of new images due to incompatible software application versions.
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Lipari Foods is recalling multiple cheeses because of a supplier's recall of cheese due to potential contamination with Listeria monocytogenes.
Product has the potential to be contaminated with Listeria monocytogenes.
Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on label.
Multiple laboratory analysis found multiple instances where various cheeses exceed allowed limits of generic E. coli.
Product has the potential to be contaminated with Listeria monocytogenes.
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Lipari Foods is recalling multiple cheeses because of a supplier's recall of cheese due to potential contamination with Listeria monocytogenes.
Multiple laboratory analysis found multiple instances where various cheeses exceed allowed limits of generic E. coli.
The firm stated that they were notified by some of their customers that their product contains metal fragments.
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Lipari Foods is recalling multiple cheeses because of a supplier's recall of cheese due to potential contamination with Listeria monocytogenes.
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Browse recent months with enough recall history for useful comparison.
