FDAJanuary 5, 2016device

T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment.

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

The hazard

Reports that the T-piece does not fit on the nebulizer.

What to do

FDA enforcement status: Terminated

Brands named

salter labssalter

Recall history

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

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