Product Wiki · Recalls · Health Canada — Medical Devices

Mobicath Bi-Directional Guiding Sheath — recall 44469

Health Canada — Medical Devices · Canada · 2017-03-10 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
44469
Date of alert
2017-03-10
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Greatbatch Medical, the manufacturer of Mobicath Bi-Directional Guiding Sheaths, is conducting a global voluntary field removal following the discovery of a pouch seal integrity issue with specific lots of Mobicath Bi-Directional Guiding Sheath, Large Curve Product (Catalogue number: d140011) and Small Curve Product (Catalogue number: d140010).
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/mobicath-bi-directional-guidin

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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