Exact FDA event identifier

Event 66031

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

Open FDA event record

Event summary

Timeline bucket: July 10, 2013
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Becton Dickinson & Company

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

BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lakes, NJ 07417 USA Made in USA. Used to perform heel sticks for the purpose of collecting skin puncture blood.

Z-2192-2013

Recall number: Z-2192-2013
Initiated: July 10, 2013
Classification: Class II
Status: Terminated
Recalling firm: Becton Dickinson & Company
Quantity: US - 39,800 units ; Canada - 18,400 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.

Code information

REF # 368101 Lot #3116007 Class I Exempt Device listing Number E158602

Distribution pattern

Distributed in the states of CT, KY, IL, NY, PA, TX, and VA and the country of Canada.