Becton Dickinson & Company recalls BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
Read the official notice →- Date
- 2025-11-26
- Country
- United States
- Brand
- Becton Dickinson &
- Product
- BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution including in the states of AL, AZ, CA,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Becton Dickinson & recalls
- 2026-06-10
USBecton Dickinson & Company recalls 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…
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 due to quality issues identified during an FDA manufacturing…
FDA · DeviceBecton Dickinson & CompanyNationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS,…Official notice →- 2026-05-06
- US
Becton Dickinson & Co. recalls BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the country of Hong Kong.Official notice → - 2026-03-18
- US
Becton Dickinson & Company recalls 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
FDA · DeviceBecton Dickinson & CompanyUS Nationwide distribution in the states of California and Texas.Official notice → - 2025-11-19
- US
Becton Dickinson & Co. recalls BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution in the states of CO, CT, KY, NJ, TN,…Official notice → - 2025-10-29
- US
Becton Dickinson & Co. recalls BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2.…
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of…
FDA · DeviceBecton Dickinson & Co.Worldwide distribution. US Nationwide including Guam and Puerto Rico, Algeria,…Official notice → - 2025-07-30
- US
Becton Dickinson & Co. recalls BD COR System Software. Model Number: 444829.
Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.
FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution in the states of Florida, Texas and…Official notice →
Other drugs & medical recalls in the United States
- 2025-11-26
- US
Medline Industries, LP recalls MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.
Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
- US
Medtronic Perfusion Systems recalls MC3 VitalFlow Console, REF 58100; Blood pump of ecmo
As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation. When this occurs, the touch screen may become temporarily unresponsive and go…
- US
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone) Model/Catalog Number: 106531US, HeartMate 3 Controller, US;…
Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.
FDA · DeviceThoratec LLCWorldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice → - US
ELEKTA SOLUTIONS AB recalls MOSAIQ Oncology Information System Software Builds 3.1.3, 3.2.1, 3.2.2 & 3.2.3.0 Software Version and UDI Codes: 3.1.3.0…
When appending a care plan that contains one or more wave medication orders, the occurrence and frequency of the appended orders may not match the intended schedule.
FDA · DeviceELEKTA SOLUTIONS ABWorldwide - U.S. Nationwide distribution in the state of NM and the countries…Official notice → - US
TMJ Solutions Inc recalls TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.
FDA · DeviceTMJ Solutions IncUS: IL, OR, MS, TX, OK, UT, MA, MD, NY, PA, VA, FL, CA, MN, GA OUS: Canada,…Official notice → - US
CareFusion 303, Inc. recalls BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100, REF: 49000270. Used…
If infusion pump is dropped or severely jarred this may damage the pump module bezel assembly, which can cause under-infusion, over-infusion, unregulated flow, or pump module failure to calibrate; so dropped/jarred…
FDA · DeviceCareFusion 303, Inc.Worldwide distribution. US nationwide including Puerto Rico, Guam, American…Official notice →