FDADecember 8, 2021device

Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.

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

The hazard

There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp.

What to do

FDA enforcement status: Terminated

Brands named

technomed europetechnomed

UPCs

0871837586170708718375867549087183758654390871837586785308718375861691087183758616840871837586154708718375866863

Recall history

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

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