UnratedMedical device recall · FDA · Published July 15, 2019
Centurion Medical: Port Access Infusion Kit 1" Needle Recall
Centurion Medical recalls Port Access Infusion Kit 1" needles due to supplier-initiated recall of GRIPPER Needles. Affected units include Product Code DYNDC2817 with specific lot numbers.
📍Recalling firmCenturion Medical Products Corporation100 Centurion Way · Williamston, MI 48895-9086
✎ GovInfoNow plain-language explainer
Centurion Medical is recalling Port Access Infusion Kit 1" needles because the supplier identified a problem with the GRIPPER Needles used in these kits. This recall affects patients who use these needles for medical infusions and could pose a risk if the needles are not properly secured. Read more at govinfonow.com/recall/67426-centurion-medical-port-access-infusion-kit-1-needle-recall.
“Centurion Medical: Port Access Infusion Kit 1" Needle Recall.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/67426-centurion-medical-port-access-infusion-kit-1-needle-recall. Based on FDA recall #Z-0256-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0256-2020%22&limit=1).
The FDA announced on July 15, 2019, that Centurion Medical Products Corporation voluntarily recalled PORT ACCESS INFUSION KIT - 1" NEEDLE (Product Code: DYNDC2817) due to supplier-initiated issues with GRIPPER Needles. The recall affects 200 kits distributed in Illinois.
How to tell if you have it
Brand: Centurion Medical
Product: PORT ACCESS INFUSION KIT - 1" NEEDLE
Product Code: DYNDC2817
Lot Number: 2019060390
Expiration Date: 11/30/2020
Quantity: 200 kits
Distribution: IL
The hazard
The recall involves GRIPPER Needles supplied for the PORT ACCESS INFUSION KIT. The record classifies this as a Class II recall.
Context
GovInfoNow's records show Centurion Medical Products Corporation has 11 other recalls on record since July 5, 2017. Other recent recalls of similar products include Medline medical kits recall (Feb. 27, 2026), Medline Centurion Kits Recall (March 19, 2026), and Braun Medical Spinal Needle Kits Recall (May 6, 2026).
How to tell if you have this one
Check for the product code DYNDC2817 on the Port Access Infusion Kit 1" needles. The lot number is listed as 2019060390 with an expiration date of November 30, 2020.
Brand
Centurion Medical
Category
Medical device
FDA recall event · 4 products
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
IL
Recall number
Product, codes & lots
Quantity
Z-0253-2020
Port full Access Tray Product Code: DT19330; Lot Number Expiration 2018092801 12/31/2019 2018121401 5/31/2020 2019022601 6/30/2020 2019032901 6/30/2020
240 kits
Z-0254-2020
Maintenance Flush Kit/Blood Draw Product Code: DT19335; Lot Number Expiration 2018110501 7/31/2021 2018121801 7/31/2021 2019013001 9/30/2021 2019032901 9/30/2021
240 kits
Z-0255-2020
Kit, Port Access Product Code: DYNDC1582A; 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
11260 kits
Z-0256-2020
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817; Lot Number Expiration 2019060390 11/30/2020
200 kits
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify the product code DYNDC2817 and lot number 2019060390 on the Port Access Infusion Kit 1" needles.
Where it went and when
Where it was distributed
Distributed in Illinois.
Listed by the agency
Not listed
FDA distribution: “IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0256-2020 (July 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0256-2020 to see it in context.
Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.