Exact FDA event identifier

Event 71674

2 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: July 09, 2015
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Cadence Inc.

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

2 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 2

Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212

Z-2364-2015

Recall number: Z-2364-2015
Initiated: July 09, 2015
Classification: Class II
Status: Terminated
Recalling firm: Cadence Inc.
Quantity: 766 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

Code information

Packged Lots: Catalog Number 5202: 79713-04, 80468-05, W003542/1, W006324/1, W006324/2, W006324/3, W006324/4, W006324/5; Catalog Number 5205: 79748-03; Catalog Number 5212: W008136/1, W008686/1, W011240/1, W010905/1, W012135/1, W014053/1, W015838/1, W011240

Distribution pattern

Nationwide Foreign Canada, Denmark. Italy

device · product 2 of 2

Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209

Z-2365-2015

Recall number: Z-2365-2015
Initiated: July 09, 2015
Classification: Class II
Status: Terminated
Recalling firm: Cadence Inc.
Quantity: 1665 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

Code information

Packged Lots: Catalog Number 5208: 79895-01, 80044-02, 82350-01, W006510/1; Catalog Number 5209: 71880-01, 76434-01, 76461-01, 76461-02, 76461-03, 76461-04, 76461-05, 76461-06, 76461-07, 76461-08, 79748-01, 80044-03, W001711/1, W002337/1, W002886/1

Distribution pattern

Nationwide Foreign Canada, Denmark. Italy