Drugs & medicalClass II

Augmedics Ltd. recalls Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation…

The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient to the user and the tightening markings found to be improperly placed.

Read the official notice →
Date
2025-05-21
Country
United States
Brand
Augmedics Ltd.
Product
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation…
Classification
Class II
Units
US Nationwide.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-05-21
  2. US
    Drugs & medicalClass II

    Contec Medical Systems Co., Ltd. recalls CMS8000 Patient Monitor

    Patient monitor has nine identified cybersecurity vulnerabilities.

    FDA · DeviceContec Medical Systems Co., Ltd.US Nationwide distribution in the states of CA, IL, FL, KY, TX.Official notice →
  3. US
    Drugs & medicalClass II

    ICU Medical, Inc. recalls LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2

    Firm has identified Drug Library Management defects in the software: 1) DLM software does not allow user to create percentage dose rate or rate change values with certain limits, potentially resulting in over-delivery…

    FDA · DeviceICU Medical, Inc.Worldwide - US Nationwide distribution in the states of CA, FL, IA, KY, LA,…Official notice →
  4. US
    Drugs & medicalClass II

    Cook Incorporated recalls Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular…

    Cook Medical identified that devices from the affected device lots may contain the incorrectly sized embolization coil.

    FDA · DeviceCook Incorporatedworldwide - No US distribution.Official notice →
  5. US
    Drugs & medicalClass II

    Numed Inc recalls BIB Balloon in Balloon Dilatation Catheter. Model Number: 420

    Balloon extension lumens are not printed correctly. Specifically, the inner balloon inflation hub was labeled as the outer balloon, and the outer balloon inflation hub was labeled as the inner balloon.

    FDA · DeviceNumed IncUS distribution to Pennsylvania.Official notice →
  6. US
    Drugs & medicalClass II

    Richard Wolf GmbH recalls PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with…

    The high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell. In extremely rare instances a…

    FDA · DeviceRichard Wolf GmbHUS State: GAOfficial notice →
  7. US
    Drugs & medicalClass II

    LeMaitre Vascular, Inc. recalls Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56

    During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).

    FDA · DeviceLeMaitre Vascular, Inc.Nationwide distribution. International distribution to ARGENTINA, AUSTRALIA,…Official notice →
See all drugs & medical recalls →