FDA Device recall Z-0796-2016
T-piece Nebulizer with in-line connectors, Part number 8915-7-50
- FDA Device
- Class II
- terminated
- Published 2016-02-17
On 2016-02-17 the FDA classified a Class II recall of T-piece Nebulizer with in-line connectors, Part number 8915-7-50 by Salter Labs, citing reports that the T-piece does not fit on the nebulizer.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0796-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-01-05 |
| Published | 2016-02-17 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Salter Labs |
| Distribution | NY, OH, PA, SC, TN, TX |
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.
Reason
Reports that the T-piece does not fit on the nebulizer.
Identifiers
| code_info | Lot No. 083115, 090715, and 122815 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0796-2016%22
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