FDAJanuary 14, 2019device

RUSCH CARE Premium Drain bag, 2000mlm REF 390000 urine collection device

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

The hazard

The device labels are not UDI compliant. The missing UDI compliance information on the labelling is not likely to affect the function/performance of the device itself. Other label information and warnings are unaffected by this labelling.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

UPCs

14026704645708

Recall history

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

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RUSCH CARE Premium Drain bag, 2000mlm REF 390000 urine collection device — Recall Details · AllClear