Product Wiki · Recalls · Health Canada — Medical Devices

RapidFlap System, 12MM - 20MM RapidFlap SpinDown Clamp (2018-10-11) — recall 58899

Health Canada — Medical Devices · Canada · 2018-11-30 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
58899
Date of alert
2018-11-30
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Zimmer Biomet is conducting a medical device recall for the spin down rapidflap for product manufactured prior to September 17, 2018 due to the nut that interfaces with the outer plate potentially being misassembled.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/rapidflap-system-12mm-20mm-rap

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