Incorrect catheter connector within the kit resulting in inability to provide a secure connection to the epidural catheter. The incorrect catheter connector is smaller than the required catheter connector and therefore is unable to be used to administer medication.
Reason for recall: Incorrect catheter connector within the kit resulting in inability to provide a secure connection to the epidural catheter. The incorrect catheter connector is smaller than the required catheter connector and therefore is unable to be used to administer medication. Distribution: US Nationwide distribution in the states of MO, OK. Quantity: 1090 units Lot/code info: UDI-DI 04046964669286 (Primary); 04046964669279 (Unit of Use); Lot Number 0061916572
04046964669286, 04046964669279
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.