FDAApril 16, 2020device

BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535

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

The hazard

This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

UPCs

50382903065535

Recall history

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

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BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535 — Recall Details · AllClear