FDAApril 21, 2017device

PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

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

The hazard

Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory — Recall Details · AllClear