Drugs & medicalClass II

Medtronic Neuromodulation recalls Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger Kit used by the RestoreUltra (Model 37712), RestoreSensor…

The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger Kits) become unresponsive if the charging steps, indicated in the Recharger Patient User Guide, are not followed.

Read the official notice →
Date
2021-12-01
Country
United States
Brand
Medtronic Neuromodulation
Product
Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger Kit used by the RestoreUltra (Model 37712), RestoreSensor…
Classification
Class II
Units
US Nationwide, including PR. There was government distribution but no military…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Medtronic Neuromodulation recalls

  1. 2022-08-31
  2. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators…

    Potential for Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 to display an Unexpected Device Error Code 1502 Message, and the user will be unable to perform programming of the Vanta Implantable…

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution including in the states of…Official notice →
  3. 2022-06-01
  4. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200

    The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution in the states of AK, AL,…Official notice →
  5. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with Surescan MRI…

    The Implantable Neurostimulator Model may be susceptible to not communicating with the clinical programmer and/or patient programmer system.

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →
  6. 2022-05-04
  7. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator, Model Numbers: 1)…

    There is a software anomaly with the InterStim X Clinician software application with results in the data entered in the Patient Information fields not e retained and a " Data Lost" notification being displayed.

    FDA · DeviceMedtronic NeuromodulationUS Nationwide distribution in the states of FL, IL, WI, TX, CA, ND, NC, KY,…Official notice →
  8. 2022-01-05
  9. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Model B35200 - Percept PC BrainSense Implantable Neurostimulator

    During cardioversion events, the Model B35200 Percept PC Implantable Neurostimulator could become unresponsive and non-functional. Cardioversion is a procedure performed by a cardiologist to correct an abnormal…

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide and Puerto Rico. The countries of…Official notice →
  10. 2021-11-10
  11. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Clinician Programmer Application (CPA) model A610 Clinician Software Application

    A software anomaly may occur with the clinician programmer application.

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution and the countries of…Official notice →
All 35 Medtronic Neuromodulation recalls →

Other drugs & medical recalls in the United States

  1. 2021-12-01
  2. US
    Drugs & medicalClass II

    Atrium Medical Corporation recalls The Ocean Water Seal Chest Drain is a plastic, three bottle vacuum collection device. It consists of a collection chamber that holds…

    Inadequate/inappropriate Set-Up Instructions, which may result in delay in treatment and an unreasonable risk of harm to the patient

    FDA · DeviceAtrium Medical CorporationUS Nationwide Distribution Foreign: Bahrain Belgium Brunei Darussalam Canada…Official notice →
  3. US
    Drugs & medicalClass II

    Becton Dickinson Infusion Therapy Systems Inc. recalls BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min…

    There is a breach in the product packaging that renders the product non-sterile.

    FDA · DeviceBecton Dickinson Infusion Therapy Systems Inc.U.S. Nationwide Distribution: AR, AZ, MA, GA, NC, OH, WA, NY, NJ, HI, CA, MD,…Official notice →
  4. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Artis Q.zen ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and…

    If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result in a short delay in procedure

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide DistributionOfficial notice →
  5. US
    Drugs & medicalClass II

    Medtronic Vascular, Inc. recalls Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE STENT GRAFT…

    Due to, during stent graft deployment, the spindle may detach from the distal end of the spindle hypotube.

    FDA · DeviceMedtronic Vascular, Inc.Worldwide distribution - U.S. Nationwide distribution in the states of CA, FL,…Official notice →
  6. US
    Drugs & medicalClass II

    Medtronic Vascular, Inc. recalls Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE

    During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube

    FDA · DeviceMedtronic Vascular, Inc.Worldwide distribution - U.S. Nationwide distribution in the states of CA, FL,…Official notice →
  7. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000

    software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in diagnosis, the necessity for patient…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide distribution.Official notice →
See all drugs & medical recalls →