Drugs & medicalClass II

Iantrek Inc. recalls C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional…

Potential for compromised integrity of the sterile packaging.

Read the official notice →
Date
2025-10-22
Country
United States
Brand
Iantrek Inc.
Product
C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional…
Classification
Class II
Units
US Nationwide distribution in the states of AL, AZ, CA, CT, DE, FL, GA, ID,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-10-22
  2. US
    Drugs & medicalClass II

    Kico Knee Innovation Company recalls Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version:…

    Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.

    FDA · DeviceKico Knee Innovation CompanyUS Nationwide distribution in the states of IN, MN, MO, OH, FL, IL, RI, KY,…Official notice →
  3. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls TENACIO Pump without InhibiZone; UPN: 72404420;

    The potential for devices to experience inflation and/or deflation performance issues or difficulties.

    FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  4. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Adult Anesthesia Set, REF DYNJ39985G

    Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of MO.Official notice →
  5. US
    Drugs & medicalClass II

    Ferno-Washington Inc recalls FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.

    The fastening post hardware could loosen allowing the fastening post to detach from the cot

    FDA · DeviceFerno-Washington IncUS Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, IS, IL,…Official notice →
  6. US
    Drugs & medicalClass II

    Insulet Corporation recalls The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field…

    The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a…

    FDA · DeviceInsulet CorporationUS Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Contego Medical LLC recalls Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP System), REF:…

    Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter that may not open or may not fully open during sheath retraction and operation of the filter knob. The…

    FDA · DeviceContego Medical LLCUS Nationwide distribution in the states of FL, CO, CA, IL, NC, KY, TX, PA,…Official notice →
See all drugs & medical recalls →