PlainRecalls

Becton Dickinson & Company

Compiled from official public sources by the editorial team.

169 recalls on record · Latest: Mar 18, 2026

Becton Dickinson & Company Recall Insight

Becton Dickinson & Company appears on 169 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.166% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Mar 18, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 2 critical, 48 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Jun 12, 2019 to May 27, 2020.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000435

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000026A

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 4F Single-Lumen, Catalog Number CK000276

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000278

FDA Devices Moderate May 27, 2020

BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000025

FDA Devices Moderate May 27, 2020

BARD MYPICC KIT 3F Single-Lumen, Catalog Number CK000417B

FDA Devices Moderate May 20, 2020

PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D

FDA Devices Moderate May 6, 2020

CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) …

FDA Devices Moderate Dec 4, 2019

Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of the human body. Site~Rite 8 Ultrasound System, Catalog No.9770500 Refu…

FDA Devices Moderate Nov 27, 2019

BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)

FDA Devices Moderate Nov 27, 2019

BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547

FDA Devices Moderate Nov 13, 2019

13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI: 00801741066023 Power-Trialysis Short-Term Alphacurve Dialysis Catheter with a…

FDA Devices Moderate Nov 13, 2019

MaxZero Extension Sets with Needle-less Connector, Product codes MZ1000 MZ1000-07 MZ5301 MZ5302 MZ5303 MZ5304 MZ5305 MZ5306 MZ5307 MZ530…

FDA Devices Moderate Nov 6, 2019

BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608

FDA Devices Moderate Oct 30, 2019

BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide…

FDA Devices Moderate Oct 16, 2019

BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985

FDA Devices Moderate Oct 16, 2019

BD Microtainer SST- Amber Part/Catalog Number: 365978

FDA Devices Moderate Oct 16, 2019

BD Microtainer SST Part/Catalog No.365967

FDA Devices Moderate Oct 16, 2019

BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog Number: 365987

FDA Devices Moderate Oct 16, 2019

BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963

FDA Devices Moderate Oct 16, 2019

BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965

FDA Devices Moderate Oct 16, 2019

BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Glycolytic Inhibitor Part/Catalog Number: 365992

FDA Devices Moderate Oct 16, 2019

BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974

FDA Devices Moderate Oct 16, 2019

CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the IV line and/or IV catheter d…

FDA Devices Moderate Sep 4, 2019

8 G x 10 CM Jamshidi Crown Bone Marrow biopsy/Aspiration Needle with MAC Catalog Number: TMJ4008

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes, Catalog Number 367886

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 367960

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes, Catalog Number 367964

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes, Catalog Number 366664

FDA Devices Moderate Aug 28, 2019

BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes, Catalog Number 368494

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes, Catalog Number 366667

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962

FDA Devices Moderate Aug 28, 2019

BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes, Catalog Number 368884

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN 75 USP Units Blood Collection Tubes, Catalog Number 367884

FDA Devices Moderate Aug 28, 2019

BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Blood Collection Tubes, Catalog Number 368035, 368036

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN (LH) 158 USP Units Blood Collection Tubes, Catalog Number 367880

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes, Catalog Number 367963

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection Tubes, Catalog Number 367961

FDA Devices Moderate Aug 21, 2019

BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol determinations

FDA Devices Moderate Jul 31, 2019

3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

FDA Devices Moderate Jul 31, 2019

3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061

FDA Devices Moderate Jul 24, 2019

BD Microtainer Tube w/ BD Microgard Closure, K2EDTA additive, Model Numbers 365974 and 365975 Product Usage: The Microtainer¿ Brand Tube with EDT…

FDA Devices Critical Jul 17, 2019

Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930, 11522558, 11607704, 10013361T, …

FDA Devices Critical Jul 3, 2019

SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696

FDA Devices Moderate Jun 12, 2019

BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.