FDA Device recall Z-0285-2016
Prism Medical P-300 Portable Consumer Lift
- FDA Device
- Class II
- terminated
- Published 2015-11-25
On 2015-11-25 the FDA classified a Class II recall of Prism Medical P-300 Portable Consumer Lift by Ergosafe Products Dba Prism Medical, citing drive shaft and over speed arm may simultaneously fail potentially resulting in a patient falling during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0285-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-09-08 |
| Published | 2015-11-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ergosafe Products Dba Prism Medical |
| Distribution | US |
Product
Prism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051; weight specification 300 lbs. /136 kg.
Reason
Drive shaft and over speed arm may simultaneously fail potentially resulting in a patient falling during use
Identifiers
| code_info | All serial numbers produced since October 2011. Part Number 303050: SN P303885 P305001 P303816 P303948 P304050 P…All serial numbers produced since October 2011. Part Number 303050: SN P303885 P305001 P303816 P303948 P304050 P304745 P303670 P303783 P303822 P304003 P303999 P303675 P303342 P303351 P303519 P303690 P303784 P304045 P303405 P305150 P303741 P303825 P303916 P304732 P303595 P303850 P304597 P304606 P305056 P305095 P303547 P304715 P305040 P304598 P303458 P303945 P304012 P304016 P304438 P304740 P303528 P303552 P303684 P304705 P303802 P303820 P303658 P305099 P304707 P303051 P303106 P303484 P303487 P303688 P303756 P303771 P303863 P303866 P303870 P303600 P303762 P303867 P305000 P303657 P303659 P305011 P303534 P303540 P304077 P303804 P303064 P303110 P303114 P303137 P303665 P303698 P303455 P303284 P304713 P304711 P304013 P303523 P303753 P304401 P304093 P304714 P303692 P303195 P304096 P303162 P303460 P304047 P303160 P303834 P303974 P303594 P305053 P305102 P303356 P303407 P303409 P304098 P303616 |
|---|
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-0285-2016%22
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