FDA Device recall Z-2122-2014
InTouch Critical Care Bed, Stryker Medical
- FDA Device
- Class II
- terminated
- Published 2014-08-06
On 2014-08-06 the FDA classified a Class II recall of InTouch Critical Care Bed, Stryker Medical by Stryker Medical Division, citing stryker has received complaints from the field alleging instances where the In Touch beds are hoisted or lifted from the floor and the casters have fallen off. The investigations….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2122-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-04 |
| Published | 2014-08-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
Reason
Stryker has received complaints from the field alleging instances where the In Touch beds are hoisted or lifted from the floor and the casters have fallen off. The investigations into these casters have shown that in these cases the caster has broken on the top of the caster stem where the brake rod inserts into the caster. If more than one caster on a unit is damaged, brake functions can be affec
Identifiers
| code_info | Model 2130 T01168 T01723 T01331 T02213 T02554 T01544 T01167 T01722 T01330 T02212 T02553 T01609 T01166 T01721…Model 2130 T01168 T01723 T01331 T02213 T02554 T01544 T01167 T01722 T01330 T02212 T02553 T01609 T01166 T01721 T01329 T02211 T02552 T01608 T01165 T01310 T01328 T02210 T02551 T01543 T01164 T02089 T01327 T02209 T02550 T02515 T01163 T01967 T01326 T02208 T02549 T02514 T01162 T01966 T01325 T02207 T02173 T02513 T01161 T01965 T01324 T02206 T02172 T01613 T01160 T01964 T01323 T02205 T02171 T01612 T02644 T01963 T01322 T02204 T02170 T01611 T02068 T01962 T01321 T02203 T02169 T01610 T02067 T01961 T01699 T02202 T02168 T02174 T02066 T01960 T01698 T02201 T02167 T02180 T02512 T01959 T01697 T02200 T02166 T02179 T02511 T01958 T01696 T02199 T01931 T02178 T02510 T01957 T01695 T02198 T01930 T02177 T02509 T01956 T01665 T02197 T01929 T02176 T02508 T01955 T01664 T02196 T01928 T02175 T02507 T01954 T01663 T02152 T01927 T01572 T02506 T01953 T01662 T01369 T01926 T01548 T01388 T01952 T01661 T01368 T01925 T01547 T01387 T01951 T02237 T01377 T01924 T01526 T01386 T01950 T02236 T01376 T01923 |
|---|
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-2122-2014%22
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