Exact FDA event identifier

Event 73130

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: January 05, 2016
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Salter Labs

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

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.

Z-0796-2016

Recall number: Z-0796-2016
Initiated: January 05, 2016
Classification: Class II
Status: Terminated
Recalling firm: Salter Labs
Quantity: 70 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Reports that the T-piece does not fit on the nebulizer.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Reports that the T-piece does not fit on the nebulizer.

Code information

Lot No. 083115, 090715, and 122815

Distribution pattern

Distributed in the states of TX, NY, PA, TN, SC, and OH, and in China.