FDA Device recall Z-2753-2018
Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another by Handicare Usa, citing premature strap wear and breakage at maximum weight conditions (625 lbs.).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2753-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-11-03 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Handicare Usa |
| Distribution | US |
Product
Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Reason
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Identifiers
| code_info | Device Model; 303090 and 303093 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2753-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.