Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1939-2015 — 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.

U.S. FDA — Device Enforcement · United States · 2015-06-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1939-2015
Date of alert
2015-06-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Sechrist Industries Inc
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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