FDA Device recall Z-0363-2014
Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable long-term care bed intended for medical purposes that consists of a bed with…
- FDA Device
- Class II
- terminated
- Published 2013-11-27
On 2013-11-27 the FDA classified a Class II recall of Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable long-term care bed intended for medical purposes that consists of a bed with… by Stryker Medical Division, citing it was reported that the siderail may appear latched when it is not, due to lack of proper preventive maintenance. This might result in bruises and/or lacerations to a patient who….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0363-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-23 |
| Published | 2013-11-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable long-term care bed intended for medical purposes that consists of a bed with a built-in motor and controls that can be operated to adjust the height and surface contour of the bed. The device includes movable and latchable siderails
Reason
It was reported that the siderail may appear latched when it is not, due to lack of proper preventive maintenance. This might result in bruises and/or lacerations to a patient who is leaning against the siderails if the siderail releases. Additionally, the siderail may not effectively constrain a patient to prevent them from rolling or falling off the bed.
Identifiers
| code_info | Model FL14E B01008 B05307 B08323 B11351 B14383 B17357 B20142 B23142 B01010 B05308 B08324 B11352 B1…Model FL14E B01008 B05307 B08323 B11351 B14383 B17357 B20142 B23142 B01010 B05308 B08324 B11352 B14384 B17358 B20143 B23143 B01022 B05309 B08325 B11353 B14385 B17358 B20144 B23144 B01045 B05310 B08326 B11354 B14386 B17359 B20145 B23145 B01045 B05311 B08327 B11355 B14387 B17359 B20146 B23146 B01323 B05312 B08328 B11356 B14388 B17360 B20147 B23147 B01356 B05313 B08329 B11357 B14389 B17360 B20148 B23148 B01392 B05314 B08330 B11358 B14390 B17361 B20149 B23149 B01433 B05315 B08331 B11359 B14391 B17361 B20150 B23150 B01434 B05316 B08332 B11360 B14392 B17362 B20151 B23151 B01465 B05317 B08333 B11361 B14393 B17362 B20152 B23152 B01466 B05318 B08334 B11362 B14394 B17363 B20153 B23153 B01467 B05319 B08335 B11363 B14395 B17363 B20154 B23154 B0147 |
|---|
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-0363-2014%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.