Recall events
/
Event 83542
Event summary
Timeline bucket July 15, 2019
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Centurion Medical Products Corporation
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
4 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 4
Port full Access Tray Product Code: DT19330
Z-0253-2020
Recall number Z-0253-2020
Initiated July 15, 2019
Classification Class II
Status Terminated
Quantity 240 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Supplier initiated recall of the GRIPPER Needles
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0253-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3515]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Supplier initiated recall of the GRIPPER Needles
Code information Lot Number Expiration 2018092801 12/31/2019 2018121401 5/31/2020 2019022601 6/30/2020 2019032901 6/30/2020
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[11334]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 4
Maintenance Flush Kit/Blood Draw Product Code: DT19335
Z-0254-2020
Recall number Z-0254-2020
Initiated July 15, 2019
Classification Class II
Status Terminated
Quantity 240 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Supplier initiated recall of the GRIPPER Needles
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0254-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39465]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Supplier initiated recall of the GRIPPER Needles
Code information Lot Number Expiration 2018110501 7/31/2021 2018121801 7/31/2021 2019013001 9/30/2021 2019032901 9/30/2021
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[7618]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 4
Kit, Port Access Product Code: DYNDC1582A
Z-0255-2020
Recall number Z-0255-2020
Initiated July 15, 2019
Classification Class II
Status Terminated
Quantity 11260 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Supplier initiated recall of the GRIPPER Needles
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0255-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51068]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Supplier initiated recall of the GRIPPER Needles
Code information Lot Number Expiration 2018121350 8/31/2020 2019020750 9/30/2020 2019031550 4/30/2021 2019041550 4/30/2021 2019061750 1/31/2021 2019062450 4/30/2021
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[11344]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 4
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Z-0256-2020
Recall number Z-0256-2020
Initiated July 15, 2019
Classification Class II
Status Terminated
Quantity 200 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Supplier initiated recall of the GRIPPER Needles
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0256-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15339]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Supplier initiated recall of the GRIPPER Needles
Code information Lot Number Expiration 2019060390 11/30/2020
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[8753]
FDA event record
· Exact recall-number query on openFDA
