FDA Device recall Z-2781-2015
NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984
- FDA Device
- Class II
- terminated
- Published 2015-09-23
On 2015-09-23 the FDA classified a Class II recall of NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984 by Salter Labs, citing the Inspiratory valve cap on the nebulizer reservoir tower may be loose and may detach before or during treatment.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2781-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-04 |
| Published | 2015-09-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Salter Labs |
| Distribution | US |
Product
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.
Reason
The Inspiratory valve cap on the nebulizer reservoir tower may be loose and may detach before or during treatment.
Identifiers
| code_info | Lot Numbers 042015 through 070615A Series 8660, 8960, 8961, 8966, 8984. Nebulizers (part numbers 8660-7, 8960-7, 8960…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). |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2781-2015%22
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