FDAAugust 28, 2024device

MEDLINE OPEN HEART NIMC KIT, REF DYNJ908840

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

The hazard

Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

4019532718507810195327185077

Recall history

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

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MEDLINE OPEN HEART NIMC KIT, REF DYNJ908840 — Recall Details · AllClear