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FDASeptember 8, 2022device

Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH, REF Number 3373-91

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

The hazard

The kits are being recalled due to a lack of sterility of a spare needle contained within the kits. There is a potential for skin infection or sepsis if the patient is exposed to a non-sterilized, unused needle.

What to do

FDA enforcement status: Terminated

Brands named

sunmed

UPCs

0070907800448310709078004480

Recall history

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

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