Carina Mobile Lifts — Class II medical device recall Z-0014-2018
Terminated recall by Handicare AB, reported 2017-10-18, distributed in MD, OH, PA. A limited amount of Carina mobile lifts have been delivered with a too small locking pin. If a locking pin sma
| Recall number | Z-0014-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Handicare AB, Lulea, Sweden |
| Recall initiated | 2016-07-28 |
| Classified | 2017-10-11 |
| Reported by FDA | 2017-10-18 |
| Terminated | 2018-12-17 |
| Distributed | MD, OH, PA |
| Quantity | 9 units |
| Serial numbers | 660900500, 660900571, 661102000, 661102160, 661200500, 661200584 |
| Model numbers | 60600009, 60600012, 6060011 |
Product
Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009
Reason for recall
A limited amount of Carina mobile lifts have been delivered with a too small locking pin. If a locking pin smaller than the correct size is mounted on the Carina mobile lift, the locking pin is likely to cause increased wear on the plastic bushings. In case of continued use, these components may cause wear on the metal of the piston rod eye.
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-0014-2018. 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.