Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap on the nebulizer reservoir...

Date: August 4, 2015
Company: Salter Labs
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Salter Labs directly.

Affected Products

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.

Quantity: 8,975

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Salter Labs

Salter Labs has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report