Stryker recalls Power-PRO 2 ambulance cots with insufficient epoxy causing head or foot sections to detach during transport. Affected units have specific serial numbers. Contact Stryker for repair or replacement.
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.
Stryker is recalling Power-PRO 2 ambulance cots that may separate during transport due to weak epoxy. This could cause injury if the cot detaches while moving a patient.
The cot's head and foot sections may separate during loading or unloading because the epoxy used to secure them is insufficient. This could cause the cot to unexpectedly detach while moving a patient, potentially leading to injury.
Ambulance crews and emergency responders using the Power-PRO 2 cot for patient transport. Those with the specific serial numbers listed are most at risk.
Check the serial numbers: 2208002066, 2208002071, 2209001508, or 2208001664. The Power-PRO 2 is an ambulance cot for transporting patients in emergencies or non-emergencies.
Look for the serial numbers listed: 2208002066, 2208002071, 2209001508, or 2208001664.
The cot's head and foot sections may separate during transport due to insufficient epoxy, which could cause injury if the cot detaches while moving a patient.
Check the serial numbers. If you have one of the listed serial numbers, contact Stryker for repair or replacement.
Yes, if the cot separates during transport, it could cause injury to the patient or responder.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1256-2023 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1256-2023 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
