Z-1256-2023 Class II Ongoing
FDA device recall Z-1256-2023 was initiated by Stryker Medical Division of Stryker Corporation on February 1, 2023 and is designated Class II. 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 unexpe… The recall status is ongoing. Affected quantity: 4 units.
Recall Details
- Product Type
- Devices
- Report Date
- March 22, 2023
- Initiation Date
- February 1, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4 units
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.
Distribution Pattern
US Nationwide distribution in the states of NY, VA.
Code Information
GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664