Product Wiki · Recalls · Health Canada — Medical Devices

Bard Access Systems trays and/or kits that contain the Aplicare Skin… — recall 57150

Health Canada — Medical Devices · Canada · 2017-10-05 · Type III

As described by Health Canada — Medical Devices: Bard Access Systems trays and/or kits that contain the Aplicare Skin Prep Pad (2017-09-12)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
57150
Date of alert
2017-10-05
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Bard is informing customers of a label change to a component in the listed Bard Access Systems (BAS) trays and/or kits. The component, Skin Prep Pad (part number p-1010), manufactured by Aplicare, Inc., will no longer be labeled as sterile (new non-sterile part number p-1030). Over the next several months, BAS will deplete inventory of the sterile-labeled product and transition to the modified labeled product in its trays and/or kits. No product return is required.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bard-access-systems-trays-ando

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.