Becton Dickinson & Company
Complete recall history across all FDA and CPSC categories — 169 total recalls
Recall Summary
Becton Dickinson & Company appears in recall records across 2 categories. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Drug Recalls (1)
FDA drug safety enforcement actions by Becton Dickinson & Company
| Date | Product | Reason | Class |
|---|---|---|---|
| Sep 15, 2017 | ChloraPrep OneStep (Clear) (2% w/v chlorhexidine gluconate (CHG) and 70% v/v ... | Labeling; Label Mixup; the immediate package is labeled incorrectly as Chloro... | Class II |
Device Recalls (168)
FDA medical device enforcement actions by Becton Dickinson & Company. Showing most recent 50.
| Date | Product | Reason | Class |
|---|---|---|---|
| Jan 27, 2026 | 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bu... | During the bulk packaging process, some Luer Slip syringes were incorrectly i... | Class II |
| Oct 14, 2025 | BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341; | BD has confirmed through internal testing that certain device trays failed ro... | Class II |
| Nov 16, 2023 | PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syri... | An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline... | Class II |
| Oct 11, 2023 | BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump In... | Affected infusion sets labeled as free of DEHP actually do contain di(2-ethyl... | Class II |
| Oct 11, 2023 | BD Extension Sets (Product Name, Catalog #) BD SmartSite Filter Extension ... | Affected infusion sets labeled as free of DEHP actually do contain di(2-ethyl... | Class II |
| Oct 11, 2023 | BD gravity sets (Product Name, Catalog #) 32-IN GRAV SET W/0.2 MICRON FILT... | Affected infusion sets labeled as free of DEHP actually do contain di(2-ethyl... | Class II |
| Feb 1, 2023 | BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml, 12.7mm, 28G Sin... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Feb 1, 2023 | BD Ultra-Fine Insulin Syringe 1mL, 6mm, 31G-Insulin Syringes are designed for... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Feb 1, 2023 | BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed ... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Feb 1, 2023 | BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml, 12. 7mm, 28G Two U... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Feb 1, 2023 | BD Ultra-Fine II Insulin Syringe 0.5mL, 8mm, 30G-Insulin Syringes are designe... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Feb 1, 2023 | BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Feb 1, 2023 | BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Singl... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Feb 1, 2023 | BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed f... | Nonsterile syringe potentially exposing the patient to pathogenic microorgani... | Class II |
| Sep 15, 2022 | BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog... | The affected product contains isobutylene which has recently demonstrated pot... | Class II |
| Jul 18, 2022 | BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Dr... | Incorrect expiration date listed on the product labels. The expiration date l... | Class II |
| May 9, 2022 | BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches... | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Catalog No.3836... | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| May 9, 2022 | BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS) | May have the potential for leakage at the housing component of the stopcock, ... | Class II |
| Jan 6, 2022 | BD Vacutainer Luer Lok Access Device - intended as a sterile, single use devi... | May shed contaminant particles into the urine specimen that may be misidentif... | Class III |
| Sep 27, 2021 | BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used... | Holes in product packaging impacts package integrity and may compromise steri... | Class II |
| Dec 23, 2020 | BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482 | The product packaging for the 10 ml eccentric tip syringe may exhibit open se... | Class II |
| Dec 9, 2020 | BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for adminis... | BD was advised by the European Notified Body, NSAI, that the instructions for... | Class II |
| Dec 9, 2020 | BD Regional Block Needles 22G x 1.50in (50 units/cs.). Indicated for administ... | BD was advised by the European Notified Body, NSAI, that the instructions for... | Class II |
| Nov 18, 2020 | BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usag... | BD has confirmed the presence of blood on the cannulas of the BD PrecisionGli... | Class II |
| Oct 23, 2020 | BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administ... | Product shelf cartons incorrectly labeled as products intended for the Latin ... | Class II |
| Sep 14, 2020 | Bard 3F SL PowerMidline Basic Kit CE-indicated for short term access to the p... | Kits do not contain the stylet/T-lock assembly indicated as a component on th... | Class II |
| Sep 14, 2020 | Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the pe... | Kits do not contain the stylet/T-lock assembly indicated as a component on th... | Class II |
| Sep 14, 2020 | BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref... | Dull/blunt needles within the IV Catheter System may lead to missed insertion... | Class II |
| Jul 28, 2020 | BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack | Printed scale markings on the 3mL SafetyGlide syringes, with catalog # 305924... | Class II |
| Jun 19, 2020 | SafeStep Huber Needle Set; Catalog Numbers LH-0029 (UDI 00801741066160), LH-... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | PowerLoc MAX Power Injectable Infusion Set with GuardIVa Antimicrobial Hemost... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | SafeStep Huber Needle Set AllPoints Port Access System; Catalog Numbers AN152... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | SafeStep Huber Needle Set myPICK Port Access Kit; Catalog Numbers CPA00020A (... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | SafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Inject... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Cata... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | PowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit; Catalog Nu... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | SafeStep Huber Needle Set Port Access Kit; Catalog Numbers PA-0029 (UDI 00801... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing Por... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | PowerLoc MAX Power Injectable Infusion Set; Catalog Numbers 0131910 (UDI 0080... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Ca... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
| Jun 19, 2020 | PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 21319... | Potential development of cracks or breaks in the tubing near the Luer or Y si... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.
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