LITe Decompression Tube Snake Arm
Brand(s)
Last updated
Summary
Product
LITe Decompression Tube Snake Arm
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| LITe Decompression Tube Snake Arm | 227764 | 48080230 |
Issue
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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Orthopaedics
Companies
Stryker Spine
2 Pearl Court, Allendale, New Jersey, United States, 07401
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74703
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