FDADecember 9, 2020device

BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect anesthesia or analgesia to a specific anatomical location (region). Catalog No. 404204

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

The hazard

BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to include the general contraindications

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

UPCs

50382904042047

Recall history

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

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