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BECTON DICKINSON AND COMPANY

United States US-MF-000018910 Last updated 23 Oct 2026

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Devices
7
Registries
EUDAMEDGUDIDFDA
FDA recalls
294 ongoing

Catalogue7

  • BD Microtainer® QuikHeel™ Lancet Ref 368102

    Class II FDA UDI Active

  • Difco Ref 223101

    Class B EUDAMEDFDA UDI Active

  • Difco Ref 225431

    Class B EUDAMEDFDA UDI Active

  • Difco Ref 211780

    Class B EUDAMEDFDA UDI Active

  • Difco Ref 222771

    Class B EUDAMEDFDA UDI Active

  • Difco Ref 225481

    Class B EUDAMEDFDA UDI Active

  • Difco Ref 228151

    Class B EUDAMEDFDA UDI Active

FDA recalls29

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

Showing the 10 most recent of 29 recalls.

  • 2026

    • 11 Aug 2026 Z-3250-2026 Class II Ongoing Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.via FDA establishment BECTON, DICKINSON AND CO.
    • 8 Apr 2026 Z-2202-2026 Class II Ongoing Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.via FDA establishment BECTON, DICKINSON AND CO.
    • 8 Apr 2026 Z-2203-2026 Class II Ongoing Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.via FDA establishment BECTON, DICKINSON AND CO.
    • 8 Apr 2026 Z-2204-2026 Class II Ongoing Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.via FDA establishment BECTON, DICKINSON AND CO.

  • 2010

    • 17 Dec 2010 Z-2159-2011 Unclassified (pre-2012) Terminated Restricted or no fluid flow for Visitec High Viscosity Injector.via FDA establishment BECTON, DICKINSON AND CO.
    • 17 Dec 2010 Z-2160-2011 Unclassified (pre-2012) Terminated Restricted or no fluid flow for Visitec High Viscosity Injector.via FDA establishment BECTON, DICKINSON AND CO.
    • 17 Dec 2010 Z-2161-2011 Unclassified (pre-2012) Terminated Restricted or no fluid flow for Visitec High Viscosity Injector.via FDA establishment BECTON, DICKINSON AND CO.
    • 17 Dec 2010 Z-2162-2011 Unclassified (pre-2012) Terminated Restricted or no fluid flow for Visitec High Viscosity Injector.via FDA establishment BECTON, DICKINSON AND CO.
    • 17 Dec 2010 Z-2163-2011 Unclassified (pre-2012) Terminated Restricted or no fluid flow for Visitec High Viscosity Injector.via FDA establishment BECTON, DICKINSON AND CO.
    • 17 Dec 2010 Z-2164-2011 Unclassified (pre-2012) Terminated Restricted or no fluid flow for Visitec High Viscosity Injector.via FDA establishment BECTON, DICKINSON AND CO.
Show the 25 most recent of 29 recalls

  • 2010

    • 4 Oct 2010 Z-0606-2011 Unclassified (pre-2012) Terminated Finger flange on the BD 1% OVD syringe can disengage during cataract surgery and and may lead to injury.via FDA establishment BECTON, DICKINSON AND CO.
    • 6 Apr 2010 Z-1597-2010 Unclassified (pre-2012) Terminated A field action was initiated due to a recent customer complaint from Japan there is a labeling mixup and that some of the BD Visitec EdgeAhead MVR Knife 0.90mm (20G), REF 585230, shelf packs may contain BD Visitec EdgeAhead Slit Knife 2.3mm (40 degree), REF 8009918.via FDA establishment BECTON, DICKINSON AND CO.

  • 2009

    • 12 Jun 2009 Z-1638-2010 Unclassified (pre-2012) Terminated Mislabeled: Arthro-Lok Pointed Tip 4mm Blade curving right instead of left.via FDA establishment BECTON, DICKINSON AND CO.

  • 2008

    • 15 Sep 2008 Z-0022-2009 Unclassified (pre-2012) Terminated Product labeled as 4 mm High Viscosity Injector tip contains a 6 mm tip.via FDA establishment BECTON, DICKINSON AND CO.
    • 7 Jul 2008 Z-2433-2008 Unclassified (pre-2012) Terminated Metal particulates present.via FDA establishment BECTON, DICKINSON AND CO.

  • 2007

    • 20 Nov 2007 Z-0453-2008 Unclassified (pre-2012) Terminated No Fluid Flow or Restricted Fluid Flow: Nucleus Hydrodissector(s) were found to have reduced or no fluid flow.via FDA establishment BECTON, DICKINSON AND CO.
    • 20 Nov 2007 Z-0454-2008 Unclassified (pre-2012) Terminated No Fluid Flow or Restricted Fluid Flow: Nucleus Hydrodissector(s) were found to have reduced or no fluid flowvia FDA establishment BECTON, DICKINSON AND CO.
    • 9 Aug 2007 Z-0066-2008 Unclassified (pre-2012) Terminated Microkeratome blade may stop oscillating and transverse the eye causing injury to the corneavia FDA establishment BECTON, DICKINSON AND CO.
    • 2 Mar 2007 Z-0672-2007 Unclassified (pre-2012) Terminated Mislabeled: Carton label incorrectly labeled as Ref 581618 (.40 X 16mm) , may contain product Ref 581617 (.50 x 16mm)via FDA establishment BECTON, DICKINSON AND CO.

  • 2006

    • 26 Dec 2006 Z-0401-2007 Unclassified (pre-2012) Terminated Product sterility may be compromised due to incomplete package sealvia FDA establishment BECTON, DICKINSON AND CO.
    • 26 Dec 2006 Z-0402-2007 Unclassified (pre-2012) Terminated Product sterility may be compromised due to incomplete package sealvia FDA establishment BECTON, DICKINSON AND CO.
    • 26 Dec 2006 Z-0403-2007 Unclassified (pre-2012) Terminated Product sterility may be compromised due to incomplete package sealvia FDA establishment BECTON, DICKINSON AND CO.
    • 26 Dec 2006 Z-0404-2007 Unclassified (pre-2012) Terminated Product sterility may be compromised due to incomplete package sealvia FDA establishment BECTON, DICKINSON AND CO.
    • 26 Dec 2006 Z-0405-2007 Unclassified (pre-2012) Terminated Product sterility may be compromised due to incomplete package sealvia FDA establishment BECTON, DICKINSON AND CO.
    • 26 Dec 2006 Z-0406-2007 Unclassified (pre-2012) Terminated Product sterility may be compromised due to incomplete package sealvia FDA establishment BECTON, DICKINSON AND CO.

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Becton, Dickinson And Co. DROGHEDA Louth · IE FEI 3005698992

Information

Country
United States
Address
7, Loveton Circle, Sparks, United States
Website
www.bd.com
PRRC contact
Megan Reeher
EUDAMED SRN
US-MF-000018910
FDA FEI number
1911916