Prism Medical C-300 Consumer Ceiling Lift — Class II medical device recall Z-0284-2016
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-0284-2016 |
|---|---|
| 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 | 561 lifts |
| Model numbers | 000014, 00010, 00011, 00012, 00013, 303163, 303283, 303330, 303333, 330050, 330050R, 330053, 330053R, 330057, C303001, C303003, C303005, C303021, C303022, C303023, C303024, C303025, C303026, C303027, C303028 and 475 more |
Product
Prism Medical C-300 Consumer Ceiling Lift; PN 330050, 330050R, 330053, 330053R, and 330057; weight specification 300 lbs. /136 kg. Lifting aid used by health care professionals to lift, position, and transfer clients or disabled family members.
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-0284-2016. 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.