T-piece Nebulizer with in-line connectors — Class II medical device recall Z-0796-2016
Terminated recall by Salter Labs, reported 2016-02-17, distributed in NY, OH, PA, SC, TN, TX. Reports that the T-piece does not fit on the nebulizer.
| Recall number | Z-0796-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Salter Labs, Carlsbad, CA, United States |
| Recall initiated | 2016-01-05 |
| Classified | 2016-02-10 |
| Reported by FDA | 2016-02-17 |
| Terminated | 2016-04-21 |
| Distributed | NY, OH, PA, SC, TN, TX |
| Countries outside the US | CN |
| Quantity | 70 units |
| Lot numbers | 083115, 090715, 122815 |
| Model numbers | 8915-7-50 |
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 for recall
Reports that the T-piece does not fit on the nebulizer.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0796-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.