Salter Labs: Medical Device Recall in 2016 - (Recall #: Z-0796-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: January 5, 2016

Date Posted: February 17, 2016

Recall Number: Z-0796-2016

Event ID: 73130

Reason for Recall:

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

Status: Terminated

Product Quantity: 70 units

Code Information:

Lot No. 083115, 090715, and 122815

Distribution Pattern:

Distributed in the states of TX, NY, PA, TN, SC, and OH, and in China.

Voluntary or Mandated:

Voluntary: Firm initiated