FDAApril 22, 2016device

15 g R.K. Epidural Needle (TW), Catalog #/REF #100-1415 Intended for the epidural placement, directly or through an epidural catheter, of anesthetic agents to elicit regional anesthesia

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a possibility that the needles may have the potential to skive a catheters outer coating. If this were to occur, there exists the risk that a portion of the catheter could remain in the patient, which may require otherwise unnecessary medical invention.

What to do

FDA enforcement status: Terminated

Brands named

epimed

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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15 g R.K. Epidural Needle (TW), Catalog #/REF #100-1415 Intended for the epidural placement, directly or through an epidural catheter, of anesthetic agents to elicit regional anesthesia — Recall Details · AllClear