FDAJuly 4, 2022device

Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD

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

The hazard

Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification

What to do

FDA enforcement status: Ongoing

Brands named

medicina ukmedicina

UPCs

05060278508146

Recall history

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

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Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD — Recall Details · AllClear