FDAJune 1, 2015device
Sechrist Low Profile Wheeled Stretcher, Model No. 21762-110-33H, 21762-110-36H, 21762-110-41H, 21762-135-33HJ, 21762-010-36H, 21762-010-41H, 21762-111-36H.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Sechrist Industries is recalling the Sechrist Low Profile Wheeled Stretcher because it may experience an unexpected incline angle during the height adjustment of the Low Profile Wheeled Stretcher when lifting the patient upward or when lowering the Wheeled Stretcher to a height at which the patient can be loaded/unloaded.
What to do
FDA enforcement status: Terminated
Brands named
sechrist
Recall history
No related federal recalls on record for this brand yet.
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