Prism Medical P-440 Portable Ceiling Lift — Class II medical device recall Z-2269-2015
Terminated recall by ErgoSafe Products, LLC (DBA) Prism Medical, reported 2015-08-05, distributed nationwide. There is a potential the sling loops may not stay attached to the carry bar hooks.
| Recall number | Z-2269-2015 |
|---|---|
| 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 | 2015-06-24 |
| Classified | 2015-07-27 |
| Reported by FDA | 2015-08-05 |
| Terminated | 2017-04-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GB, JP, KR |
| Quantity | 7,105 lifts |
Product
Prism Medical P-440 Portable Ceiling Lift; PN 303070 and 303070R (refurbished); Patient lift with weight specification of 440 lbs (200 kg). Product Usage: The P-440 lift is a lifting aid used by health care professionals and those providing care in the home to lift, position, and transfer clients or a disabled family member. The ceiling lift makes it possible to move mobility impaired individuals with minimal strain or risk to the caregiver, while providing complete safety, dignity, and comfort for the client or family member.
Reason for recall
There is a potential the sling loops may not stay attached to the carry bar hooks.
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-2269-2015. 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.