Salter Labs: Medical Device Recall in 2015 - (Recall #: Z-2781-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984. Nebulizer used to generate aerosols delivered directly to the patient for breathing. Designed to be used in either a hospital or homecare environment.

Product Classification:

Class II

Date Initiated: August 4, 2015

Date Posted: September 23, 2015

Recall Number: Z-2781-2015

Event ID: 71909

Reason for Recall:

The Inspiratory valve cap on the nebulizer reservoir tower may be loose and may detach before or during treatment.

Status: Terminated

Product Quantity: 8,975

Code Information:

Lot Numbers 042015 through 070615A Series 8660, 8960, 8961, 8966, 8984. Nebulizers (part numbers 8660-7, 8960-7, 8960TG-7, 8967-7, 8982-7, 8984-7), Inspiratory valve cap (part number 600116).

Distribution Pattern:

Worldwide Distribution - US Nationwide and in the countries of Greece, UK, Belgium, Australia, and Switerzland.

Voluntary or Mandated:

Voluntary: Firm initiated