Class II — Sechrist Industries Inc
| Recalling firm | SECHRIST INDUSTRIES, INC. |
|---|---|
| Registered facility | SECHRIST INDUSTRIES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Product | 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. |
| Quantity | 81 US Distribution |
| Distribution | US Distribution and Internationally to Japan and Jordan. |
| Initiated | 2015-06-01 |
| Classified | 2015-06-30 |
| Terminated | 2015-10-20 |
| Recall number | Z-1939-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Sechrist Industries Inc (Z-1939-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71455/
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