Recall Z-1939-2015— Sechrist Industries Inc
Class II · Terminated
Class II FDA medical device recall by Sechrist Industries Inc, initiated 2015-06-01, terminated 2015-10-20. FDA's recall record names no specific 510(k) clearance for this event. 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.. 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..
- Recalling firm
- Sechrist Industries Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-06-01
- Terminated
- 2015-10-20
- Firm location
- Anaheim, CA, United States
Product description
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.
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.