Prism Medical P-300 Portable Consumer Lift — Class II medical device recall Z-0285-2016
Terminated recall by ErgoSafe Products, LLC (DBA) Prism Medical, reported 2015-11-25, distributed nationwide. Drive shaft and over speed arm may simultaneously fail potentially resulting in a patient falling during use
| Recall number | Z-0285-2016 |
|---|---|
| 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 | 2015-09-08 |
| Classified | 2015-11-17 |
| Reported by FDA | 2015-11-25 |
| Terminated | 2017-05-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GB, JP, KR, MX, TW |
| Quantity | 1,721 lifts |
| Model numbers | 303050, 303050R, 303051, 303332, 303475, 303617, 303618, 303619, 303620, 303621, 303622, 303623, 303624, 303751, 517420, C303033, C303091, C303097, C303137, C303139, C303144, C303146, C303148, C303151, C303152 and 475 more |
Product
Prism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051; weight specification 300 lbs. /136 kg.
Reason for recall
Drive shaft and over speed arm may simultaneously fail potentially resulting in a patient falling during use
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-0285-2016. 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.