Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
FDA Recall Z-0479-2023 · Posted 2022-12-14
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Recalling FirmStryker Medical Division of Stryker Corporation
Recall StatusOpen, Classified
Product CodeFPO
Date Initiated2022-11-11
Product Quantity465 (403 US; 62 OUS)
Reason for Recall
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
Firm Action
On November 11, 2022, the firm notified affected customers via "URGENT:
MEDICAL DEVICE CORRECTION" letters. Devices require servicing. Customers were instructed to locate affected units and identify the address where they can be serviced. Until servicing can be performed, customers were provided with additional instructions and precautions to follow to ensure safe continued use of the device. Return the enclosed business reply form to confirm receipt of this notification by fax +1 269 488 8691 or email [email protected]. Upon receipt of the completed business reply form, Stryker will contact you to arrange for the modification/repair of your Power-PRO 2. If you have loaned or sold any of the products listed in this letter, please forward a copy of this notice to the new users and advise us of their new location in the space provided on the business reply form.
If you have any questions or concerns, contact Customer Service at +1 800 327 0770 Monday through Friday from 8:00 a.m. to 6:00 p.m. ET.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide Distribution: US (Nationwide) and Foreign to countries of: Australia, Canada, Netherlands, and United Kingdom.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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