Becton Dickinson & Company
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
- Becton Dickin…
Becton Dickinson & Co.
185 notices
- Chevrolet
Chevrolet
183 notices
- Becton Dickin… (this)
Becton Dickinson & Company
179 notices
- Medline Indus…
Medline Industries Inc.
179 notices
- Albertsons Co…
Albertsons Companies LLC
175 notices
- Working Cow H…
Working Cow Homemade Inc.
175 notices
What this shows Becton Dickinson & Company holds about 0.171% of archive notices alongside 179 distinct filings.
How the 179 notices break down
Same federal filing book as the hero total — split by issuing agency, no new counts.
FDA Devices Moderate Jul 29, 2020
PowerLoc MAX Power Injectable Infusion Set; Catalog Numbers 0131910 (UDI 00801741047329), 0131915 (UDI 00801741047336), 0131975 (UDI 00801741047343), 0132010 (UDI 00801741047350), 0132015 (UDI 00801741047367), 0132075 (UDI 00801741047374), 0132210 (UDI 00801741047381), 0132215 (UDI 00801741047398), 0132275 (UDI 00801741047404), 0141910 (UDI 00801741047411), 0141915 (UDI 00801741047428), 0141975 (UDI 00801741047435), 0142010 (UDI 00801741047442), 0142015 (UDI 00801741047459), 0142075 (UDI 00801
FDA Devices Moderate Jul 29, 2020
SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers PA-0031G (UDI 00801741085666), PA-0031YNG (UDI 00801741085673), PA-0032G (UDI 00801741087639), PA-0033G (UDI 00801741096433)
FDA Devices Moderate Jul 29, 2020
SafeStep Huber Needle Set Port Access Kit; Catalog Numbers PA-0029 (UDI 00801741085482), PA-0029YN (UDI 00801741085499), PA-0030 (UDI 00801741085505), PA-0030YN (UDI 00801741085512), PA-0031 (UDI 00801741085529), PA-0031YN (UDI 00801741085536), PA-0032 (UDI 00801741085543), PA-0032YN (UDI 00801741085550), PA-0033 (UDI 00801741085567), PA-0033YN (UDI 00801741085574), PA-0034 (UDI 00801741085581), PA-0034YN (UDI 00801741085598), PA-0036 (UDI 00801741085604), PA-0038 (UDI 00801741085628), PA-0038YN
FDA Devices Moderate Jul 29, 2020
PowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit; Catalog Numbers CPA00001 (UDI 00801741098345), CPA00002 (UDI 00801741098352), CPA00028 (UDI 00801741129728), CPA00032 (UDI 00801741137501), CPA00033 (UDI 00801741137501), CPA00036 (UDI 00801741138911), CPA00051 (UDI 00801741175718), CPA00055 UDI 00801741182181), CPA00056 (UDI 00801741182907)
FDA Devices Moderate Jul 29, 2020
PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224)
FDA Devices Moderate Jul 29, 2020
SafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Injection Cap; Catalog Numbers LH-0029YN (UDI 00801741066177), LH-0030YN (UDI 00801741066191), LH-0031YN (UDI 00801741066214), LH-0032YN (UDI 00801741066238), LH-0033YN (UDI 00801741066252), LH-0034YN (UDI 00801741066276), LH-0035YN (UDI 00801741066290 ), LH-0036YN (UDI 00801741066313), LH-0037YN (UDI 00801741066337), LH-0038YN (UDI 00801741066351), LH-0039YN (UDI 00801741066313), LH-0040YN (UDI 00801741066399)
FDA Devices Moderate Jul 29, 2020
SafeStep Huber Needle Set myPICK Port Access Kit; Catalog Numbers CPA00020A (UDI 00801741129827), CPA00042A (UDI 00801741182969), CPA00049 (UDI 00801741175695)
FDA Devices Moderate Jul 29, 2020
SafeStep Huber Needle Set AllPoints Port Access System; Catalog Numbers AN152075 (UDI 00801741119484), AN152075G (UDI 00801741119583), AN162010 (UDI 00801741119682), AN162010G (UDI 00801741119446), AN162075 (UDI 00801741119675), AN162075G (UDI 00801741119439)
FDA Devices Moderate Jul 29, 2020
PowerLoc MAX Power Injectable Infusion Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers 2132010G (UDI 00801741095504), 2132015G (UDI 00801741095511), 2141910G (UDI 00801741095542), 2142010G (UDI 00801741085680), 2142015G (UDI 00801741085680), 2142210G (UDI 00801741085680)
FDA Devices Moderate Jul 29, 2020
SafeStep Huber Needle Set; Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382)
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) 210930(10)0001304986
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 Refurbished, Site~Rite¿ 8 System, Catalog No.9770500R Site~Rite 8 Ultrasound System, Catalog No.9770501 Refurbished Site~Rite¿ 8 System,Catalog No.9770501R Site~Rite 8 Ultrasound System, Catalog No. 9770550 Site~Rite 8 Ultrasound System, Catalog No. 9770552 Site~Rite 8 Ultrasound System, Catalog No. 9770553 Site~Rite 8 Ultrasound System, Catalog N
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 third internal umen for IV therapy, power injection of contrast media, and central venous pressure monitoring.
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 MZ5309 MZ5310 MZ5312 MZ5313 MZ5316 MZ8001 MZ8002 MZ8003 MZ9266 MZ9267 MZ9272 MZ9273 MZ9274 MZ9275 MZ9276 MZ9277 MZ9278 MZ9279 MZ9280 MZ9281 MZ9283 MZ9287 MZ9288 MZ9289 MZ9290 MZ9292 MZ9293 MZ9294 MZ9300 MZ9301 MZ9302 MZ9313 MZ9323 MZ9324 MZ9325 MZ9326 MZ9327 MZ9329 MZT1003 MZT1004 MZX5
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 customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD Vacutainer¿ Push Button Blood Collection Set with the needle protector removed prior to needle retraction.
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 during IV therapy Cat. No. MP1000-C
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
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).
Similar medical devices volume
Nearest multi-notice firms that share this firm's dominant product category.
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