FDAOctober 16, 2024device

MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20

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

The hazard

The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

10889942358311408899423583121088994235832840889942358329

Recall history

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

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MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20 — Recall Details · AllClear