CLASS II ONGOING Device recall · Reported 22 Mar 2023 · FDA Enforcement Report
Power-PRO 2 . Intended as an ambulance cot to transport recalled
Stryker Medical Division of Stryker is recalling Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency, distributed nationwide in the US. The recall was initiated on 1 Feb 2023 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1256-2023
- FDA event ID
- 91716
- Recalling firm
- Stryker Medical Division of Stryker, Portage, MI
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 1 Feb 2023
- FDA classified
- 15 Mar 2023
- Reported
- 22 Mar 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 1 Feb 2023 | Recall initiated by company | |
| 15 Mar 2023 | Classified by FDA | +42 days |
| 22 Mar 2023 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Product as listed by the FDA
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Where it was distributed
US Nationwide distribution in the states of NY, VA.
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664
Where was it sold?
US Nationwide distribution in the states of NY, VA.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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