Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–4 of 4 recalls
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned.…
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned.…
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned.…
During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top…