Recall events
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Event 68874
Event summary
Timeline bucket July 17, 2014
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Genesis BPS, LLC.
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
Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis BPS, LLC The intended use is to prepare and deliver small aliquots of filtered whole blood, red blood cells, platelets, plasma, and cryoprecipitate for pediatric and or neonatal transfusion
Z-2667-2014
Recall number Z-2667-2014
Initiated July 17, 2014
Classification Class II
Status Terminated
Quantity 7560 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2667-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[54273]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
Code information Cat #405-530BD Lot #3640-23476; 3640-23506; 3640-24153; 3640-24206; 3640-24398; 3640-24485; 3640-24517; 3640-23969; 3640-24330; 3640-24521
Distribution pattern Nationwide Distribution & Switzerland
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[17393]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 3
Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only Genesis BPS, LLC The intended use is to prepare and deliver small aliquots of filtered whole blood, red blood cells, platelets, plasma, and cryoprecipitate for pediatric and or neonatal transfusion
Z-2668-2014
Recall number Z-2668-2014
Initiated July 17, 2014
Classification Class II
Status Terminated
Quantity 7272 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2668-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[8047]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
Code information Cat #405-560BD Lot # 3650-23508; 3650-24116; 3650-24332; 3650-24399; 3650-24487; 3650-24519; 3650-23478; 3650-23971 Cat # 405-560MJ Lot #3630-23509; 3630-23972; 3630-24181; 3630-24333; 3630-24397; 3630-24488; 3630-24152
Distribution pattern Nationwide Distribution & Switzerland
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[20915]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 3
Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS, LLC The intended use is to prepare and deliver small aliquots of filtered whole blood, red blood cells, platelets, plasma, and cryoprecipitate for pediatric and or neonatal transfusion.
Z-2669-2014
Recall number Z-2669-2014
Initiated July 17, 2014
Classification Class II
Status Terminated
Quantity 4608 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2669-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[43223]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
Code information Cat #405-535MJ Lot # 3650-23970; 3650-24518; 3650-23477; 3650-23507; 3650-24331; 3650-24396; 3650-24486; 3650-25301
Distribution pattern Nationwide Distribution & Switzerland
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[16665]
FDA event record
· Exact recall-number query on openFDA
