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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71614

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

Open FDA event record

Event summary

Timeline bucket
June 30, 2015
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Remel 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

PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. Latex agglutination test for identification of beta-hemolytic streptococci of Lancefield Groups A, B, C, F or G from primary culture plates.

Z-2350-2015
Recall number
Z-2350-2015
Initiated
June 30, 2015
Classification
Class II
Status
Terminated
Recalling firm
Remel Inc
Quantity
1859 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.

Code information

lot 1470133, exp. date 31 Mar 2016

Distribution pattern

Nationwide Distribution, including Puerto Rico and the country of Canada.

device · product 2 of 2

PathoDx Strep B Grouping Latex, REF 62031, 3 ml packaged in plastic dropper bottle with a pink cap. Latex reagent for streptococcal group B; Identify beta-hemolytic streptococci of Lancefield Groups A, B, C, F and G from primary culture plates.

Z-2351-2015
Recall number
Z-2351-2015
Initiated
June 30, 2015
Classification
Class II
Status
Terminated
Recalling firm
Remel Inc
Quantity
4420 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.

Code information

lot 1463129, exp. date 31 May 2016

Distribution pattern

Nationwide Distribution, including Puerto Rico and the country of Canada.