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FDAJune 26, 2024device

ENT RES 100 ML Non-Sterile W CLAMP, TUBING FLAG, & FEMALE LUER, Product Code 68-2230-28

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

The hazard

Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.

What to do

FDA enforcement status: Ongoing

Brands named

smiths medical asdsmithssmiths medical

UPCs

30610586044179

Recall history

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

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