C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420…
Due to stain present on the surface of affected foley catheters.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 469–480 of 4,550 recalls
Due to stain present on the surface of affected foley catheters.
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.
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.
Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to procedural delay and…