Product Wiki · Recalls · Health Canada — Medical Devices

Feather-Flex Non-Conductive Adult Anesthesia Circuit (2021-04-16) — recall 62378

Health Canada — Medical Devices · Canada · 2021-04-29 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
62378
Date of alert
2021-04-29
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: On April 15, 2021, it was discovered internally at BOMImed that during the manufacturing process, a very small number of corrugated tubes were damaged leading to a leaking tube. Out of caution, BOMImed is notifying customers and providing replacement circuits from the affected batch.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/feather-flex-non-conductive-ad

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.

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