FDA Device recall Z-0284-2016
Prism Medical C-300 Consumer Ceiling Lift
- FDA Device
- Class II
- terminated
- Published 2015-11-25
On 2015-11-25 the FDA classified a Class II recall of Prism Medical C-300 Consumer Ceiling 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-0284-2016 |
| 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 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
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 330050: SN C303094 C303510 C303374 C303922 C303924 C303925 C…All serial numbers produced since October 2011. Part 330050: SN C303094 C303510 C303374 C303922 C303924 C303925 C303257 C303386 C303223 C303264 C303492 C303239 C303352 C303326 C304076 C303429 C303847 C303457 C303065 303333 C303095 C303136 C303149 C303158 C303190 C303194 C303168 C304108 C303481 C303907 C303430 C303349 C303301 C303302 C303195 C303378 C303897 C303271 C303159 C303362 C303234 C303058 C303068 C304082 C303392 C303895 C303900 C303341 C303060 C303235 C303023 p303952 C303024 C303005 C303057 C303086 C303090 C303092 C303118 C303138 C303140 C303141 C303142 C303152 C303154 C303155 C303161 C303163 C303191 C303192 DEMOC002 DEMOC010 C303025 C303026 C303196 C303238 C303241 C303245 C303021 C303067 C303391 C303143 C303153 C303226 C303304 C303385 C303495 C303393 C303432 C303237 C303476 C303323 C303361 C303363 C303366 C303389 C303321 C303344 C303943 C304057 C303381 C303419 C303451 C303263 |
|---|
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-0284-2016%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.