Drugs & medicalClass I

Medtronic Heart Valves Division recalls Medtronic Harmony Delivery Catheter System

Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a…

Read the official notice →
Date
2026-07-08
Country
United States
Brand
Medtronic Heart Valves Division
Product
Medtronic Harmony Delivery Catheter System
Classification
Class I
Units
Worldwide distribution - US Nationwide and the countries of Argentina,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2026-07-08
  2. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper Back…

    The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the Upper Back Section H V U component on Baxter operating…

    FDA · DeviceBaxter Healthcare CorporationWorldwide - US Nationwide distribution in the states of Minnesota, Maryland,…Official notice →
  3. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls CRE Pro Wireguided 12-15mm 240cm

    Potential sterile breach of the pouches in which devices are packaged.

    FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →
  4. US
    Drugs & medicalClass II

    Hamilton Medical AG recalls IntelliCuff, Portable automatic cuff pressure controller REF: 951001

    Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.

    FDA · DeviceHamilton Medical AGWorldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA,…Official notice →
  5. US
    Drugs & medicalClass II

    Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460

    Reduced or no recovery of some strains of Neisseria gonorrhoeae.

    FDA · DeviceRemel, IncWorldwide distribution - US Nationwide and the countries of Canada, Singapore,…Official notice →
  6. US
    Drugs & medicalClass I

    Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit

    Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

    FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of PA, GA, CA, WA.Official notice →
  7. US
    Drugs & medicalClass II

    Medacta Usa Inc recalls Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974,…

    Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size…

    FDA · DeviceMedacta Usa IncUS Nationwide distribution in the states of CO, AR, IN, PA, UT, FL.Official notice →
See all drugs & medical recalls →