Hollister Incorporated recalls AnchorFast Guard
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 721–732 of 801 recalls
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Medline is recalling medical convenience kits which were assembled with specific Coloplast Foley catheters and Prostatic catheters which were subsequently recalled due to a potential sterility issue detected during testi…
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.