Recall events
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Event 79687
Event summary
Timeline bucket March 20, 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
3 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 3
BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12 (Catalog no 367342)
Z-1531-2018
Recall number Z-1531-2018
Initiated March 20, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1531-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[21495]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
Code information 7354908 8005794 8005795 8005796 8010728 8010732 8012784 8012844 8012848 8018509 8019702
Distribution pattern US (Nationwide) Canada, Kuwait, Guyana, Guatemala, Taiwan, UK, Belgium, Sweden, Ireland, Israel, Spain, Switzerland and Lithuania
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26198]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 3
BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 mm x 305 mm 21G x ¿ x 12 Catalog 367344
Z-1532-2018
Recall number Z-1532-2018
Initiated March 20, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1532-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38956]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
Code information 7346627 7348974 7348975 7354740 7354743 7354745 7354764 8005556 8005557 8005814 8010735 8012910 8015923 8015925
Distribution pattern US (Nationwide) Canada, Kuwait, Guyana, Guatemala, Taiwan, UK, Belgium, Sweden, Ireland, Israel, Spain, Switzerland and Lithuania
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[21768]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 3
BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12. Catalog no 367364
Z-1533-2018
Recall number Z-1533-2018
Initiated March 20, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1533-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51467]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
Distribution pattern US (Nationwide) Canada, Kuwait, Guyana, Guatemala, Taiwan, UK, Belgium, Sweden, Ireland, Israel, Spain, Switzerland and Lithuania
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[21734]
FDA event record
· Exact recall-number query on openFDA
