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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79709

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

Open FDA event record

Event summary

Timeline bucket
February 13, 2018
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

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

BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983

Z-2055-2018
Recall number
Z-2055-2018
Initiated
February 13, 2018
Classification
Class II
Status
Terminated
Quantity
9,568,900 total products

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube

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

Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube

Code information

1) UDI DI (01)50382903679831 PI (17)180531(10)7135828(30)1000 Lot/Serial # 7315828 Exp Date 5/31/2018 2) UDI DI (01)50382903679831 PI (17)180531(10)7146901(30)1000 Lot/Serial # 7125692 Exp Date 4/30/2018

Distribution pattern

US Nationwide, Argentina, Belize , Brazil, Canada, China, Guam, India, Japan, Mexico, Nicaragua, Pakistan, Philippines, Singapore, Suriname, Taiwan

device · product 2 of 2

BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold, Catalog No. 367986

Z-2056-2018
Recall number
Z-2056-2018
Initiated
February 13, 2018
Classification
Class II
Status
Terminated
Quantity
9,568,900 total products

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube

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

Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube

Code information

UDI DI (01)50382903679862 Lot/Serial# 7146901 Exp Date 5/31/2018

Distribution pattern

US Nationwide, Argentina, Belize , Brazil, Canada, China, Guam, India, Japan, Mexico, Nicaragua, Pakistan, Philippines, Singapore, Suriname, Taiwan