FDA Device recall Z-2269-2015
Prism Medical P-440 Portable Ceiling Lift
- FDA Device
- Class II
- terminated
- Published 2015-08-05
On 2015-08-05 the FDA classified a Class II recall of Prism Medical P-440 Portable Ceiling Lift by Ergosafe Products Dba Prism Medical, citing there is a potential the sling loops may not stay attached to the carry bar hooks.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2269-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-24 |
| Published | 2015-08-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ergosafe Products Dba Prism Medical |
| Distribution | US |
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
There is a potential the sling loops may not stay attached to the carry bar hooks.
Identifiers
| code_info | All serial numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2269-2015%22
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