Stryker Medical Division of Stryker Corporation ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450. Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450.
Brand
Stryker Medical Division of Stryker Corporation
Lot Codes / Batch Numbers
UDI-DI (GTIN): 07613327541304 . Serial number: 2212000205
Products Sold
UDI-DI (GTIN): 07613327541304 . Serial number: 2212000205
Stryker Medical Division of Stryker Corporation is recalling ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450. due to Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Recommended Action
Per FDA guidance
A customer notification was sent October 20, 2023 via FedEx. Users are to (1) Locate affected units and identify the address where they can be serviced. (2) Return the business reply form by fax +1 269 488-8691 or email to productfieldaction@stryker.com. Upon receipt of the completed business reply form, Stryker will contact you to arrange a time to complete the required electrical tests. (3) Forward notification to any new user/location and advise Stryker of the new address or device status if disposed of or obsolete using the reply form. Address questions or concerns to Customer Service at +1 800 327-0770 Monday through Friday from 8:00 a.m. to 6:00 p.m. ET.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026