Becton Dickinson & Company: 67 recalls on record

Recalls filed with 1 agency: FDA (67).

First recall on record: December 26, 2012. Most recent: June 10, 2026.

Risk classification: Class I: 11 · Class II: 54 · Class III: 2

Most recent recalls

DateAgencyProduct
June 10, 2026FDABD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivaca…Z-2251-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivaca…Z-2257-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivaca…Z-2255-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; …Z-2253-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivaca…Z-2256-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivaca…Z-2254-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacai…Z-2250-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivaca…Z-2252-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacai…Z-2248-2026
June 10, 2026FDABD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacai…Z-2249-2026
January 24, 2024FDAPosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10m…Z-0736-2024
July 27, 2022FDABD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)Z-1432-2022
July 27, 2022FDABD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)Z-1433-2022
November 4, 2020FDABard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral ven…Z-0295-2021
October 28, 2020FDABD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538…Z-0125-2021
July 29, 2020FDAPowerLoc MAX Power Injectable Infusion Set; Catalog Numbers 0131910 (UDI 00801741047329),…Z-2670-2020
July 29, 2020FDASafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Catalog Number…Z-2667-2020
July 29, 2020FDAPowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit; Catalog Numbers CPA000…Z-2661-2020
July 29, 2020FDASafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit…Z-2668-2020
July 29, 2020FDASafeStep Huber Needle Set Port Access Kit; Catalog Numbers PA-0029 (UDI 00801741085482), …Z-2666-2020
July 29, 2020FDASafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Injection Cap; Cat…Z-2669-2020
July 29, 2020FDAPowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers …Z-2660-2020
July 29, 2020FDAPowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 0080…Z-2662-2020
May 27, 2020FDABARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277Z-2078-2020
November 27, 2019FDABD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)Z-0500-2020

Questions about this company

How many recalls does Becton Dickinson & Company have?
Recalert has 67 U.S. recalls on record for Becton Dickinson & Company, published between December 26, 2012 and June 10, 2026.
What was the most recent Becton Dickinson & Company recall?
FDA recall Z-2251-2026, published June 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.
Which agencies have handled Becton Dickinson & Company recalls?
Becton Dickinson & Company appears as the recalling firm in recalls from: FDA (67).

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