Official recall record
LITe Decompression Tube Snake Arm
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2023-12-06
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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