InTouch Critical Care Bed, Stryker Medical
Medical device recall Z-2122-2014. Published in FDA’s Enforcement Report on Aug 6, 2014.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Aug 6, 2014. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 49 states named
- 11,632 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
11,632 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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…
Every code shown here, 1,996 characters
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 T01525 T01385 T01949 T02235 T01375 T01922 T02660 T01384 T01948 T02234 T01374 T01921 T02659 T02077 T02239 T02233 T01373 T01920 T02090 T02076 T02256 T02232 T01372 T01919 T02088 T02075 T02255 T02231 T01371 T01918 T01971 T01720 T02087 T02230 T01370 T01917 T01970 T01719 T02086 T02229 T01689 T01916 T01933 T01718 T01348 T02228 T01688 T01915 T01419 T02065 T01347 T02227 T01687 T01914 T01418 T02064 T01346 T02226 T01686 T01913 T01417 T02063 T01345 T02225 T01685 T01912 T01416 T02062 T01344 T02224 T01684 T01911 T01415 T02061 T01343 T02223 T01683 T01910 T01414 T02060 T01342 T02222 T01682 T01909 T01413 T02059 T01341 T02221 T02564 T01908 T01412 T02058 T01340 T02220 T02563 T01907 T01411 T02016 T01339 T02219 T02090 T01906 T01410 T02015 T01338 T02218 T02088 T01905 T01409 T02014 T01337 T02217 T01555 T01551 T01408 T02013 T01336 T02216 T01554 T01550 T01407 T02012 T01335 T02215 T01553 T01546 T01406 T02011 T01332 T02214 T01552 T01545 T01405 T01401 T02566 T02565 T01404 Model 2131 U04413 U03329 U08829 U51367 U06561 U01013 U04412 U03328…
FDA’s list runs to 81,076 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide Distribution -USA (nationwide) including DC and the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI & WV, and the countries of Argentina, Brazil, Canada, Chile, China, EMEA, Greece, Italy, Japan, Korea, Latin America, Mexico, Poland, Singapore, South Africa, Taiwan, and UK.
The states and territories these words name
49 states and territories.
Every one of them
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- District of Columbia
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jun 4, 2014.
- FDA classified it on Jul 28, 2014.
- FDA’s Enforcement Report published it on Aug 6, 2014.
- FDA terminated it on Mar 14, 2016.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Stryker Medical Division of Stryker Corporation, of Portage, MI.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 81,076 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.