Product Wiki · Recalls · Health Canada — Medical Devices

LITe Decompression Tube Snake Arm — recall 74703

Health Canada — Medical Devices · Canada · 2023-12-06 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
74703
Date of alert
2023-12-06
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Orthopaedics
Product type
Medical devices
Reported risk: Stryker received one (1) complaint for a LITe Decompression Tube Snake Arm that did not fit on to the arm post shaft that mounts to the hospital bed. Subsequent investigation determined a portion of one lot of the LITe Decompression Tube Snake Arm was manufactured with the incorrect clamp component. As a result, the affected snake arms cannot attach to the arm post shaft. No adverse events have been reported for this issue. Recall start date: November 20, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/lite-decompression-tube-snake-

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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