Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003, 110004,
The angiographic guidewire components associated with this recall are manufactured with a requirement that further downstream processing (sterilization) is required. Indications for use for these components are not defined as they are not intended for final use.
Recall Date: May 4, 2021
Mfg Country:
United States
Recall ID: 87952
Product ID: 187503
Enforcement Date: Jun 23, 2021
Last Published: Jun 30, 2021
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Emert Number: Z-1860-2021
Emert Status: Updated