Drugs & medicalClass I

Haimen Shengbang Laboratory Equipment Co. Ltd. recalls HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type

Distributed VTM outside of VTM Guidance and without clearance.

Read the official notice →
Date
2022-08-17
Country
United States
Brand
Haimen Shengbang Laboratory Equipment Co. Ltd.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type
Classification
Class I
Units
Worldwide distribution - US Nationwide distribution in the states of CA, FL,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2022-08-17
  2. US
    Drugs & medicalClass II

    Alere San Diego, Inc. recalls The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL cholesterol,…

    Cholesterol test cassettes package insert is to be updated with new bilirubin interference information because it was found that samples containing bilirubin, at concentrations greater than 2.0 mg/dL (conjugated) or…

    FDA · DeviceAlere San Diego, Inc.US: IL, NV, FL, LA, CA, MA, MN, NC, AK, NE, TX, PA, RI, SC, TN, OK, KY, GA,…Official notice →
  3. US
    Drugs & medicalClass II

    Guangdong Haiou Medical Apparatus Co., Ltd recalls Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 (0.6x25mm). 200pcs/Box Intended Use: Disposable…

    Complaints received in which needle and needle holder have detached from the syringe after injection as well as needle not retracting into the syringe as per intended use, resulting in an increased risk of needle stick…

    FDA · DeviceGuangdong Haiou Medical Apparatus Co., LtdUS Nationwide distribution in the state of CA.Official notice →
  4. US
    Drugs & medicalClass I

    Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Crome Implantable Cardioverter Defibrillators: a. Crome VR ICD, Model Numbers: DVPC3D1, DVPC3D4; b.…

    There is the potential for reduced shock energy (~79% of programmed energy) during high-voltage (HV) therapy for Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy…

    FDA · DeviceMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)Worldwide DistributionOfficial notice →
  5. US
    Drugs & medicalClass III

    Teva Pharmaceuticals USA Inc recalls Azacitidine for Injection 100mg/vial Lyophilized Powder, Rx Only, Mfd. in Romania By: Sindan Pharma SRL For BluePoint Laboratories,…

    Subpotent Drug - Out of specification (OOS) result obtained during monitoring stability study for Assay. Results below specification.

    FDA · DrugTeva Pharmaceuticals USA IncDistributed in OhioOfficial notice →
  6. US
  7. US
    Drugs & medicalClass II

    Strides Pharma Inc. recalls Prednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd., Bengaluru - 562106, India,…

    Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets

    FDA · DrugStrides Pharma Inc.US NationwideOfficial notice →
See all drugs & medical recalls →