Z-1355-2012

Stryker Critical Care Bed Model 2031, 230 V , 50/60 Hz, Max Load = 225 Kg,, Stryker, Portage, MI

Name: Z-1355-2012 Stryker Critical Care Bed Model 2031, 230 V , 50/60 Hz, Max Load = 225 Kg,, Stryker, Portage, MI
Creator: Stryker Medical Division of Stryker Corporation
Published: 2012-03-12
License: https://open.fda.gov/license/

Stryker Medical / initiated 2012-03-12 / Terminated / root cause: manufacturing process

FDA source

Stryker Medical Division of Stryker Corporation began a recall of Stryker Critical Care Bed Model 2031, 230 V , 50/60 Hz, Max Load = 225 Kg,, Stryker, Portage, MI Product Usage: EPIC II (model 2031 ) Critical Care beds... on 2012-03-12. The reason FDA records is "Stryker Medical has determined that units manufactured between September 1, 2004 through November 30, 2007, did not receive updated preventive maintenance information. (Failure to maintain the bed brakes including the...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-1355-2012
Status: Terminated
Initiated: 2012-03-12
Posted: 2012-03-30
Terminated: 2013-08-29
Recalling firm: Stryker Medical
Product: Stryker Critical Care Bed Model 2031, 230 V , 50/60 Hz, Max Load = 225 Kg,, Stryker, Portage, MI Product Usage: EPIC II (model 2031 ) Critical Care beds Med/Surg beds are AlC powered hospital beds, intended for clinician use, which consist of built-in motors and remote controls that can be operated by the patient and/or clinician to adjust the height and surface contour of the beds. The EPIC II model is primarily used in a Critical Care environment, but may be used in Med/Surg environments. Model 2031 represent International Voltage configurations of the 2030 model respectively.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: Stryker Medical has determined that units manufactured between September 1, 2004 through November 30, 2007, did not receive updated preventive maintenance information. (Failure to maintain the bed brakes including the brake plate kits, may result in reduced brake holding force. Reduced braking force may result in a patient fall or caregiver muscle strain, either of which may require medical int
Root cause tag: manufacturing process
FDA root cause: Component change control
Action: Stryker Medical sent an Urgent-Medical Device Correction letter dated March 12, 2012 to all consignees. The letter identified the affected products, problem, updated preventive maintenance information and requested the following immediate actions: 1) Locate the beds listed in this notice, 2) Ensure that the brakes are holding properly, 3) If the brakes are not holding, contact Stryker (1-800-327-0770, option 4) to order the maintenance parts, 3) Continue to periodically inspect brake functionality, as noted on enclosed preventive maintenance schedule/checklist, 4) Order replacement brake components, as needed, 5) Return the enclosed post card to confirm receipt of this notification, 6) If you have loaned or sold any of the beds listed in this letter, please, forward a copy of this notice to the new users and advise us of their new location, 6) If you have disposed of any of the beds and they are no longer in use, please, advise us of their obsolescence by providing us with their serial numbers. For questions or concerns, please, contact Sandy Cliche at 269-389-6025.
Quantity in commerce: 507
Distribution: Worldwide Distribution - USA (nationwide) including the states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY and the countries of: DEDEDO GU, HAMILTON ON, SANTIAGO, SHATIN, NT , CAPITOL FEDERAL, ITAPEVI SP, ATHENS, OSAKA, SEOUL, MEXICO DF MX, MONTREUX, BALERNA, NORTH POINT, WARSZAWA, CANOVANAS, KOWLOON BAY, SINGAPORE, NEWBURY, and JOHANNESBURG.
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Product code FNL

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)