Carry bar which is an accessory to a lift used for patients in… — Class II medical device recall Z-0728-2017
Terminated recall by ErgoSafe Products, LLC (DBA) Prism Medical, reported 2016-12-21, distributed nationwide. The black plastic puck on the carry bar is breaking resulting in potential for patient harm.
| Recall number | Z-0728-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ErgoSafe Products, LLC (DBA) Prism Medical, Maryland Heights, MO, United States |
| Recall initiated | 2016-08-30 |
| Classified | 2016-12-09 |
| Reported by FDA | 2016-12-21 |
| Terminated | 2018-07-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GB, JP, KR, TH |
| Quantity | 17,964 units |
| Model numbers | 360741, 360750, 360751, 360755, 360756, 360757 |
Product
Carry bar which is an accessory to a lift used for patients in hospitals and other facilities. Recall impacts the following model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757.
Reason for recall
The black plastic puck on the carry bar is breaking resulting in potential for patient harm.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0728-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.