Power-PRO 2 Cot (Stryker) – Insufficient Epoxy (2023)
Insufficient epoxy volume may cause unexpected disengagement during patient transport.
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
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Brand
Stryker Medical Division of Stryker Corporation
Lot Codes / Batch Numbers
GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664
Products Sold
GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664
Stryker Medical Division of Stryker Corporation is recalling Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-eme due to Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.
Recommended Action
Per FDA guidance
Stryker issued Urgent Medical Device Correction letter dated 2/1/23. Letter states reason for recall, health risk and action to take: 1. Locate the units listed on the attached business reply form and remove them from service until repairs are complete. 2. Return the enclosed business reply form to confirm receipt of this notification by fax +1 269 488 8691 or email productfieldaction@stryker.com. 3. Stryker will contact you to arrange for the modification/repair of your Power-PRO 2. 4. If you have loaned or sold or disposed of 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. 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.
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