FDAOctober 14, 2015device

Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the peritoneal cavity.

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

The hazard

The defective component can cause gas leakage through the device. This can result in loss of pneumoperitoneum, potentially necessitating removal of the defective device and insertion of another device.

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.

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