FDA DeviceClass IINotable
FDA Recall: FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-0
Description
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Hazard
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Remedy
190
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