Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0796-2016 — 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.

U.S. FDA — Device Enforcement · United States · 2016-01-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0796-2016
Date of alert
2016-01-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Salter Labs
Product category
device
Product type
Devices
Reported risk: Reports that the T-piece does not fit on the nebulizer.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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