Stryker Medical Div. of Stryker Corporation: Stryker InTouch 1.0 Critical Care Bed (Model 2130) with the Integrated PositionPro mattress (Model 2920) option. The device is intended to be used as an Intensive Care Unit bed.

Recall number

Z-0942-2009

Recalling firm

Stryker Medical Div. of Stryker Corporation

Product

Stryker InTouch 1.0 Critical Care Bed (Model 2130) with the Integrated PositionPro mattress (Model 2920) option. The device is intended to be used as an Intensive Care Unit bed.

Status

Terminated

Initiated

2009-01-05

Posted

2009-02-25

Terminated

2010-11-05

Reason

The touch screen on the footboard may display a "tilt over range" error, resulting in a precautionary stop of the bed motions which result in the bed appearing to have locked out some of its bed positioning features. Also, the "hold" button, used to interrupt an intended patient turn on beds with an integrated PositionPro mattress, may only function intermittently, resulting in an inability to ho

Root cause

Device Design

Action

Consignees were notified of the problems via letter dated January 5, 2009, advised to check their beds and to take them out of service if the foot board touchscreen displayed a "tilt over range" error, and that a Stryker Medical field service representative would contact them to perform software upgrades on the affected beds. Please direct questions to Stryker Medical at 1-269-324-6644.

Quantity

1,288 of all models

Distribution

Worldwide Distribution including USA and countries of Canada, Japan and Switzerland.

Lot, serial or model codes

Serial Numbers: T02152, T02196, T02197, T02198, T02199, T02200, T02201, T02202, T02203, T02204, T02205, T02206, T02207, T02208, T02209, T02210, T02211, T02212, T02213, T02214, T02215, T02216, T02217, T02218, T02219, T02220, T02221, T02222, T02223, T02224, T02225, T02226, T02227, T02228, T02229, T02230, T02231, T02232, T02233, T02234, T02235, T02236, T02237, T01905, T01906, T01907, T01908, T01909, T01910, T01911, T01912, T01913, T01914, T01915, T01916, T01917, T01918, T01919, T01920, T01921, T01922, T01923, T01924, T01925, T01926, T01927, T01928, T01929, T01930, T01931, T01699, T01948, T01949, T01950, T01951, T01952, T01953, T01954, T01955, T01956, T01957, T01958, T01959, T01960, T01961, T01962, T01963, T01964, T01965, T01966, T01967, T01682, T01683, T01684, T01685, T01686, T01687, T01688, T01689, T01543, T01608, T01609, T01718, T01719, T01720, T02075, T02076, T02077, T02239, T02174, T01310, T01721, T01722, T01723, T02011, T02012, T02013, T02014, T02015, T02016, T02058, T02059, T02060, T02061, T02062, T02063, T02064, T02065, T01335, T01336, T01337, T01338, T01339, T01340, T01341, T01342, T01343, T01344, T01345, T01346, T01347, T01348, T01321, T01322, T01323, T01324, T01325, T01326, T01327, T01328, T01329, T01330, T01331, T01332, T01610, T01611, T01612, T01613, T02513, T02514, T02515, T01661, T01662, T01663, T01664, T01665, T01525, T01526, T01384, T01385, T01386, T01387, T01388, T02506, T02507, T02508, T02509, T02510, T02511, T02512, T02066, T02067, T02068, T01370, T01371, T01372, T01373, T01374, T01375, T01376, T01377, T01572, T01368, T01369, T02166, T02167, T02168, T02169, T02170, T02171, T02172, T02173, T01156, T01547, T01548,  T01696, T01552, T01553, T01554, T01555, T02175, T02176, T02177, T02178, T02179, T02180, T02090, T02088, T01546, T01544, T02087, T01698, T02089, T01551, T01697, T01545, T01550 and T01695.

510(k) numbers

not on file

PMA numbers

not on file

Product code

FNL

Firm FEI

1831750

Firm city

Portage

Firm state

MI

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Copy