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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 65089

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

Open FDA event record

Event summary

Timeline bucket
April 12, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Becton Dickinson & Co.

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

BBL DrySlide PYR Kit, catalog number 231747 Product Usage: Presumptive diagnostic aid for group A streptococci and group D enterococci bacteria.

Z-1422-2013
Recall number
Z-1422-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Becton Dickinson & Co.
Quantity
610 total test kits (PYR and Oxidase)

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
incorrect packaging

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Mixed-up of materials/components

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.

Code information

PYR kit - lot 2276481 with expiration date 09/30/13

Distribution pattern

Worldwide Distribution - USA Nationwide and tthe countries of Australia, Canada, Europe, Hong Kong, Mexico, New Zealand, Singapore, and Taiwan.

device · product 2 of 2

BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.

Z-1423-2013
Recall number
Z-1423-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Becton Dickinson & Co.
Quantity
610 total test kits (PYR and Oxidase)

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
incorrect packaging

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Mixed-up of materials/components

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.

Code information

Oxidase kit - lot 2222008 with expiration date 08/31/13

Distribution pattern

Worldwide Distribution - USA Nationwide and tthe countries of Australia, Canada, Europe, Hong Kong, Mexico, New Zealand, Singapore, and Taiwan.