Recall Z-1406-2017— ErgoSafe Products, LLC (DBA) Prism Medical
Class II · Terminated
Class II FDA medical device recall by ErgoSafe Products, LLC (DBA) Prism Medical, initiated 2017-01-30, terminated 2017-12-04. FDA's recall record names no specific 510(k) clearance for this event. Product: A-series lift - A625 Manual Part No. 324117. Prism Medical.. Reason: During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely..
- Recalling firm
- ErgoSafe Products, LLC (DBA) Prism Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-01-30
- Terminated
- 2017-12-04
- Firm location
- Maryland Heights, MO, United States
Product description
A-series lift - A625 Manual Part No. 324117. Prism Medical.
Reason for recall
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Data sourced from openFDA. This site is unofficial and independent of the FDA.