Recall archive
78 recalls · page 1 of 4
Reported 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…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
Matched: Brand — This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is…
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline Flush Syringes with General Pump Compatibility. The use of BD PosiFlush…
FDA (openFDA device enforcement)
Reported Nov 29, 2023
BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 22, 2023
BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2022
BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — The affected product contains isobutylene which has recently demonstrated potential interference in determination of methanol by gas chromatography…
FDA (openFDA device enforcement)
Reported Aug 24, 2022
BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate…
10 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Company
Matched: Brand — May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i…
FDA (openFDA device enforcement)
Reported Nov 3, 2021
BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Holes in product packaging impacts package integrity and may compromise sterility.
FDA (openFDA device enforcement)
Reported Feb 24, 2021
BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — The product packaging for the 10 ml eccentric tip syringe may exhibit open seals. An open seal impacts package integrity and potentially compromises…
FDA (openFDA device enforcement)
Reported Feb 3, 2021
BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to include the general contraindications
1 more product in this recall
FDA (openFDA device enforcement)
Reported 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…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — BD has confirmed the presence of blood on the cannulas of the BD PrecisionGlide needles 30G X 1/2" Lot No. 9128897. The possibility of infection may…
FDA (openFDA device enforcement)
Reported Dec 9, 2020
BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Product shelf cartons incorrectly labeled as products intended for the Latin American market. Although the product description on the label 32G x 4mm…
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Bard 3F SL PowerMidline Basic Kit CE-indicated for short term access to the peripheral venous system for selected…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.
1 more product in this recall
FDA (openFDA device enforcement)
Reported 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…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Dull/blunt needles within the IV Catheter System may lead to missed insertion attempts and delay in diagnosis or treatment until a new needle is…
FDA (openFDA device enforcement)
Reported Sep 2, 2020
BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Printed scale markings on the 3mL SafetyGlide syringes, with catalog # 305924, Lot# 8289599, are printed incorrectly. The scale is skewed to…
FDA (openFDA device enforcement)
Reported Jul 29, 2020
PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (UDI 00801741118968),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause…
11 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2020
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
8 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Iincorrectly packaged without the required lidocaine as labeled
FDA (openFDA device enforcement)
Reported May 6, 2020
CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of the human body. Site~Rite 8 Ultrasound…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — The indicator may show available charge when the battery is close to depletion. As a result, the Site~Rite 8 has the potential to abruptly shut down,…
FDA (openFDA device enforcement)
Reported Nov 27, 2019
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
Matched: Brand — Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal…
1 more product in this recall
FDA (openFDA device enforcement)
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