Data Foundry

Medical device recalls 2014

InTouch Critical Care Bed — Class II medical device recall Z-2122-2014

Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2014-08-06, distributed nationwide. Stryker has received complaints from the field alleging instances where the In Touch beds are hoisted or lifte

Recall numberZ-2122-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Medical Division of Stryker Corporation, Portage, MI, United States
Recall initiated2014-06-04
Classified2014-07-28
Reported by FDA2014-08-06
Terminated2016-03-14
DistributedNationwide (US)
Countries outside the USAR, BR, CA, CL, CN, GB, GR, IT, JP, KR, MX, PL, SG, TW, ZA
Quantity11,632 units
Model numbers2130, 2131, 2140, 2141, 2151, 2152, 2155, 2156, T002182, T002183, T01001, T01002, T01003, T01004, T01005, T01006, T01007, T01008, T01009, T01010, T01011, T01012, T01014, T01015, T01016 and 475 more

Product

InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2122-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.