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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Centurion Medical Products Corporation: Supplier initiated recall of the GRIPPER Needles

Agency Publication Date: October 31, 2019
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Affected Products

Product: 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

Lot Numbers:
Number
Product: 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

Lot Numbers:
Number
Product: 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

Lot Numbers:
Number
Product: PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817

Lot Number Expiration 2019060390 11/30/2020

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 83542
Status: Resolved
Manufacturer: Centurion Medical Products Corporation
Manufactured In: United States
Units Affected: 4 products (240 kits; 240 kits; 11260 kits; 200 kits)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.