Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–12 of 23 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.…
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.