Drugs & medicalClass II

Becton Dickinson & Company recalls BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes…

Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.

Read the official notice →
Date
2023-03-22
Country
United States
Brand
Becton Dickinson &
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes…
Classification
Class II
Units
Worldwide distribution - US Nationwide and the countries of Chile, Colombia,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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

  1. 2023-07-12
  2. US
    Drugs & medicalClass II

    Becton Dickinson & Co. recalls BD Synapsys Informatics Solution, Catalog Number 444150

    There is a risk of mis-association of patient demographic data for users who choose to report results manually when their Service Control Unit (SCU) is operating near capacity and are using save actions (Skip, Final…

    FDA · DeviceBecton Dickinson & Co.US States: CA, CO, IA, IL, MI, MN, MO, NY, OH, OK, SC, TN, TX, UT, WI.…Official notice →
  3. 2023-06-14
  4. US
    Drugs & medicalClass II

    Becton Dickinson & Co. recalls BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B, 30 Single Use Test Devices- Intended for the in vitro, simultaneous…

    IFU- Instructions for Use (IFU) package insert and both the IFU packaged with the test kit and the electronic version on the BD website not approved by FDA,specifically describing specimen type, could cause use of the…

    FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of CA, CL, HK, TW.Official notice →
  5. 2023-04-26
  6. US
    Drugs & medicalClass II

    Becton Dickinson & Co. recalls BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software version 5.1 and 5.1.1 as part of the Icefall A platform. An in vitro…

    Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as part of the Icefall A platform, plate information was not visible in Synapsys" after processing has occurred. This could possibly lead to a…

    FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution in the states of IL, NY and the…Official notice →
  7. 2022-12-21
  8. US
    Drugs & medicalClass II

    Becton Dickinson & Co. recalls BBL Chocolate II Agar- IVD for the isolation and cultivation of Neisseria species. Catalog (Ref) Number: 221267

    Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide and does not provide enough of the blood factors necessary to support Haemophilus growth. The reduction could cause a false negative result for…

    FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of Canada, India,…Official notice →
  9. 2022-11-23
  10. US
    Drugs & medicalClass II

    Becton Dickinson & Co. recalls BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most aerobic and facultative…

    Misformulated minocycline-can cause erroneously increased Minimal Inhibitory Concentration (MIC) values when performing antibiotic susceptibility testing (AST) against minocycline and result in the reporting of false…

    FDA · DeviceBecton Dickinson & Co.US Nationwide distribution.Official notice →
  11. 2022-10-26
  12. US
    Drugs & medicalClass II

    Becton Dickinson & Company recalls BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting,…

    The affected product contains isobutylene which has recently demonstrated potential interference in determination of methanol by gas chromatography methods. The interference may lead to false positive results in…

    FDA · DeviceBecton Dickinson & CompanyDistribution US nationwide, Canada, New Zealand, and Hong Kong.Official notice →
All 36 Becton Dickinson & recalls →

Other drugs & medical recalls in the United States

  1. 2023-03-22
  2. US
    Drugs & medicalClass II

    Scientia Vascular, Inc. recalls Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090

    Microcatheters for embolic coil and diagnostic agent introduction to peripheral/neuro vasculature, due to manufacturing non-conformance, and due to flush, guidewire insertion and manipulation prior to placement, may…

    FDA · DeviceScientia Vascular, Inc.US Nationwide distribution in the states of IL, AL, FL, NC, WI, GA, SC, IN,…Official notice →
  3. US
    Drugs & medicalClass II

    Synthes (USA) Products LLC recalls TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Intended for temporary fixation and stabilization of proximal femur…

    TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length, and TFNA Femoral Nails labeled and etched as 170mm may measure 200mm in length

    FDA · DeviceSynthes (USA) Products LLCWorldwide - US Nationwide distribution in the states of MS, OR, TX and the…Official notice →
  4. US
    Drugs & medicalClass II

    Maquet Cardiovascular, LLC recalls Fusion Bioline Vascular Graft, Part number M00201503046B0

    One (1) Fusion Bioline Vascular graft from lot 25162546, which failed guideline straightness testing, was intermingled with lot 25162549 and distributed to customers. Use of the affected graft may result in reduction…

    FDA · DeviceMaquet Cardiovascular, LLCUS Nationwide distribution in the states of FL, IN, LA, MI, MO, NC, NV, NY,…Official notice →
  5. US
    Drugs & medicalClass II

    OMM Imports, Inc. dba Zero Gravity recalls Recreo Hair Growth Laser Comb

    The firm distributed the laser products without affixing the warning, aperture, certification, and identification labels. In addition, the firm failed to provide safety information, reproductions and locations of the…

    FDA · DeviceOMM Imports, Inc. dba Zero GravityWorldwide and Nationwide including DC and Puerto RicoOfficial notice →
  6. US
    Drugs & medicalClass I

    Avanos Medical, Inc. recalls BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics, Elbow Manifold.

    Potential for product manifold to crack during use on patients, possibly causing leaks in the respiratory circuit and can lead to the patient receiving inadequate ventilation.

    FDA · DeviceAvanos Medical, Inc.US Nationwide distribution in the state of Oklahoma.Official notice →
  7. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA Inc recalls Clear Eyes, Once Daily, Eye Allergy Itch Relief, olopatadine hydrochloride ophthalmic solution, USP, 0.2%, Antihistamine, 2.5 mL…

    Failed Impurities Specification: Out-of-specification (OOS) stability test result was obtained for unspecified impurity.

    FDA · DrugTeva Pharmaceuticals USA IncNationwide in the U.S.A.Official notice →
See all drugs & medical recalls →