PlainRecalls

Becton Dickinson & Company

Compiled from official public sources by the publisher.

179 recalls on record · Latest: Jun 10, 2026

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Agency notice ledger

Federal filing book Becton Dickinson & Company HEAVY-BOOK · MULTI-AGENCY

#85 of 14,151 · 179 notices · 0.171% archive

  • BOOK 179 notices
  • RANK #85 of 14,151
  • SHARE 0.171% archive
  • AGENCY FDA Devices (178)
  • CAT medical devices
  • CATS 2 categories
  • LATEST Jun 10, 2026
  • PHOTO Medline Industries In…

Nearest notice-volume peer: Medline Industries Inc. (0 notice gap)

Becton Dickinson & Company accounts for about 0.171% of the 104,423-notice archive on 179 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Becton Dickinson & Company compares to 14,151 recalling firms

Becton Dickinson & Company ranks 85th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Becton Dickinson & Company vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

179 85th of 14151 higher than 14,065 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Becton Dickinson & Company in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Becton Dickinson & Company holds about 0.171% of archive notices alongside 179 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026

How the 179 notices break down

Same federal filing book as the hero total — split by issuing agency, no new counts.

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
FDA Devices Moderate Mar 18, 2026

10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
FDA Devices Moderate Nov 26, 2025

BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
FDA Devices Moderate Jan 24, 2024

PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
FDA Devices Moderate Nov 29, 2023

BD gravity sets (Product Name, Catalog #) 32-IN GRAV SET W/0.2 MICRON FILTER BAG ACCESS PORT SS VALVE TEXIUMTM LOW ABSORPTION, Catalog # 4030B-07T and BD GRAVITY BLOOD SET 15 DROP 180 MICRON FILTER SmartSiteTM VALVE NONVENTED, Catalog # 42081E.
FDA Devices Moderate Nov 29, 2023

BD Extension Sets (Product Name, Catalog #) BD SmartSite Filter Extension Set PE lined Standard bore 1 SmartSite bonded 0.2um Large PES Filter 1 PC RLL. L: 16 in PV: 4mL, Catalog # 10013902 BD EXTENSION SET TRI-PORT SMALLBORE TUBING CHECK VALVE 3 SmartSite" VALVES, Catalog # 20062E; BD SECONDARY SET VENTED NONVENTED 20 DROP W/ 2 HANGERS, Catalog # 70000N-07; BD MaxGuardTM tri-fuse extension set, Catalog # ME1224; BD 20-IN EXTENSION SET W/ 0.2 MICRON FILTER ONE SmartSiteTM VALVE AND
FDA Devices Moderate Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore Tubing, Catalog # 10010483; BD AlarisTM Pump Infusion Set 1.2 Micron Filter Low Sorbing Tubing (PE Lined) SmartSiteTM Y-site, Catalog # 10010453; BD AlarisTM Pump Infusion Set 0.2 Micron Filter Low Sorbing Tubing (PE Lined) SmartSiteTM Y-site, Catalog # 10010454; BD AlarisTM Pump Infusion Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSiteTM Y-sites, Catalog #

FDA Devices Moderate Mar 22, 2023

BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326713
FDA Devices Moderate Mar 22, 2023

BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Single Unit Scale-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329461
FDA Devices Moderate Mar 22, 2023

BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326679
FDA Devices Moderate Mar 22, 2023

BD Ultra-Fine II Insulin Syringe 0.5mL, 8mm, 30G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326725
FDA Devices Moderate Mar 22, 2023

BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml, 12. 7mm, 28G Two Unit Scale- Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329424
FDA Devices Moderate Mar 22, 2023

BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719
FDA Devices Moderate Mar 22, 2023

BD Ultra-Fine Insulin Syringe 1mL, 6mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326678
FDA Devices Moderate Mar 22, 2023

BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml, 12.7mm, 28G Single Unit Scale. Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329420
FDA Devices Moderate Oct 26, 2022

BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.
FDA Devices Moderate Aug 24, 2022

BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the transfer of environmental contaminants into the system and the escape of drug or vapor concentrations outside the system. Catalog Number: 515304
FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)
FDA Devices Moderate Jul 27, 2022

Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
FDA Devices Moderate Jul 27, 2022

Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Catalog No.383682 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)
FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
FDA Devices Low Mar 2, 2022

BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog Number: 364902, 36490200
FDA Devices Moderate Nov 3, 2021

BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container closure integrity throughout the shelf life of the BD WWD syringe. Catalog Number: 305822
FDA Devices Moderate Feb 24, 2021

BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
FDA Devices Moderate Feb 3, 2021

BD Regional Block Needles 22G x 1.50in (50 units/cs.). Indicated for administration of medications to affect anesthesia or analgesia to a specific anatomical location (region). Catalog No. 408348
FDA Devices Moderate Feb 3, 2021

BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect anesthesia or analgesia to a specific anatomical location (region). Catalog No. 404204
FDA Devices Moderate Dec 23, 2020

BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the body below the surface of the skin.
FDA Devices Moderate Dec 9, 2020

BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge contained in a drug pen injector Catalog Number: 320122
FDA Devices Moderate Nov 4, 2020

Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media Ref: P6153208
FDA Devices Moderate Nov 4, 2020

Bard 3F SL PowerMidline Basic Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media Ref: P6153118
FDA Devices Moderate Oct 28, 2020

BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter systems are intended to be inserted into a patient s vascular system for short term use to sample blood, monitor blood pressure, or administer fluids.
FDA Devices Moderate Sep 2, 2020

BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
FDA Devices Moderate Jul 29, 2020

PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 00801741044151), 2131915 (UDI 00801741044168), 2131975 (UDI 00801741044175), 2132010 (UDI 00801741044151), 2132015 (UDI 00801741044199), 2132075 (UDI 00801741044205), 2132210 (UDI 00801741044212), 2132275 (UDI 00801741044236), 2141910 (UDI 00801741044243), 2141915 (UDI 00801741044250), 2141975 (UDI 00801741044267), 2142010 (UDI 00801741044274), 2142015 (UDI 00801741044281), 2142075 (UDI 00801741044298), 2142210

FDA Devices Moderate Jul 29, 2020

SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Catalog Number CPA00040 (UDI 00801741143892)

Becton Dickinson & Company carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (179 here — heavy-book).

Medline Industries Inc. 179 Chevrolet 183 Albertsons Companies LLC 175 Working Cow Homemade Inc. 175 Becton Dickinson & Co. 185

Similar medical devices volume

Nearest multi-notice firms that share this firm's dominant product category.

Medline Industries Inc. 179 Becton Dickinson & Co. 185 CareFusion 303, Inc. 173 Avid Medical, Inc. 172

Frequently Asked Questions

How many federal recall notices name Becton Dickinson & Company? ▼
PlainRecalls indexes 179 distinct federal recall events naming Becton Dickinson & Company, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Becton Dickinson & Company sit among other recalling firms? ▼
Becton Dickinson & Company ranks #85 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Becton Dickinson & Company's notices? ▼
FDA Devices accounts for 178 of this firm's 179 indexed notices across 2 issuing agencies.
What product category dominates Becton Dickinson & Company's filing book? ▼
Filings for Becton Dickinson & Company span 2 product categories, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Becton Dickinson & Company: 179 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Becton Dickinson & Company; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026