Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Reported: March 22, 2023 Initiated: February 1, 2023 #Z-1256-2023
Product Description
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
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.
Details
- Recalling Firm
- Stryker Medical Division of Stryker Corporation
- Units Affected
- 4 units
- Distribution
- US Nationwide distribution in the states of NY, VA.
- Location
- Portage, MI
Frequently Asked Questions
What product was recalled? ▼
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001. Recalled by Stryker Medical Division of Stryker Corporation. Units affected: 4 units.
Why was this product 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 agency issued this recall? ▼
This recall was issued by the FDA Devices on March 22, 2023. Severity: Moderate. Recall number: Z-1256-2023.
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