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FDAJuly 16, 2021device

RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 c) 112082060 d) 112082065 e) 112082070 f) 112082075 g) 112082080 h) 112082085 i) 112082090 j) 112082095 k) 112082100

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

The hazard

The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.

What to do

FDA enforcement status: Completed

Brands named

teleflex medical europeteleflexteleflex medical

Recall history

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

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RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 c) 112082060 d) 112082065 e) 112082070 f) 112082075 g) 112082080 h) 112082085 i) 112082090 j) 112082095 k) 112082100 — Recall Details · AllClear