Home / Recalls / Medical Devices
Salter Labs recalls T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device d
Recalled February 17, 2016 · FDA recall Z-0796-2016 · Salter Labs
Hazard
Reports that the T-piece does not fit on the nebulizer. · FDA Class II
Units
70 units
Sold at
Distributed in the states of TX, NY, PA, TN, SC, and OH, and in China.
Description
Reports that the T-piece does not fit on the nebulizer.
Product
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.
Manufacturer(s)
Salter Labs
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →