Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 745–756 of 801 recalls
The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.