Health product recall

LITe Decompression Tube Snake Arm

Brand(s)
Last updated

Summary

Product
LITe Decompression Tube Snake Arm
Issue
Medical devices - Performance issue
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