Drugs & medicalClass II

Alcon Research, LLC recalls Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom Paks are surgical…

Due to complaints of particulates, residue, occlusions, and bent tips for sterile cannulas.

Read the official notice →
Date
2024-05-01
Country
United States
Brand
Alcon Research
Product
Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom Paks are surgical…
Classification
Class II
Units
Worldwide distribution - U.S. Nationwide including in the states of AK, AR,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Alcon Research recalls

  1. 2024-08-28
  2. US
    Drugs & medicalClass II

    Alcon Research LLC recalls Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number: 8065992561 Software Version: N/A Product Description:…

    Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.

    FDA · DeviceAlcon Research LLCDomestic: Nationwide Distribution Countries Affected: Argentina, Australia,…Official notice →
  3. 2024-07-24
  4. US
    Drugs & medicalClass II

    Alcon Research LLC recalls Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399

    After surgery initiation, while using surgical image guidance, if significant eye rotation/movement occurs, a software anomaly may cause re-establishment of incorrect new registration angle, range indicator will…

    FDA · DeviceAlcon Research LLCWorldwide - US Nationwide distribution including in the states of AL, AR, CA,…Official notice →
  5. 2024-06-05
  6. US
    Drugs & medicalClass II

    Alcon Research LLC recalls ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic…

    Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Corneal/Scleral V-Lance Ophthalmic knives.

    FDA · DeviceAlcon Research LLCWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →
  7. 2024-04-03
  8. US
    Drugs & medicalClass II

    Alcon Research, LLC recalls SYRINGE,BULB,2OZ/60CC,GREEN, Part: 300055070, packaged inside Alcon Custom-Pak Surgical Procedure Packs, Products: 18018-06, 3865-44,…

    Medline Bulb irrigation syringes recalled due to potential for packaging sterile barrier to be breached, and these syringes were packed inside surgical procedure packs that were subsequently terminally sterilized, so…

    FDA · DeviceAlcon Research, LLCUS Nationwide distribution in the states of OH, WV.Official notice →
  9. 2023-11-15
  10. US
    Drugs & medicalClass II

    Alcon Research, LLC recalls Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG CTR

    Custom surgical procedure packs contain latex gloves but are labeled as "latex free".

    FDA · DeviceAlcon Research, LLCUS: VA OUS: NoneOfficial notice →
  11. 2023-10-18
  12. US
    Drugs & medicalClass II

    Alcon Research, LLC recalls Constellation Vision System, REF: 8065751150

    Ophthalmic microsurgical vision systems have a new Printed Circuit Board (PCB) design that could lead to higher voltage to a PCB component, that could cause component failure and loss of pressure control for the use of…

    FDA · DeviceAlcon Research, LLCUS: GA, IL, PROfficial notice →
All 22 Alcon Research recalls →

Other drugs & medical recalls in the United States

  1. 2024-05-01
  2. US
    Drugs & medicalClass I

    ROUTE 92 MEDICAL INC recalls Route 92 Medical, 070 Access System, REF 1004, Rxonly , Sterile EO. Used for introduction of interventional devices into the…

    Their is the potential for distal tip separation at the proximal marker band of the delivery catheters

    FDA · DeviceROUTE 92 MEDICAL INCUS: AL AZ CA DE FL GA IA IL IN KY LA MA MD MI MN MO NC ND NJ NY OH OR PA RI SD…Official notice →
  3. US
    Drugs & medicalClass II

    Zimmer, Inc. recalls NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

    Out of specification violation of devices that results in a gap existing within the fixture that presses the fiber metal pad to the substrate, causing the pad to not fully bond to the substrate.

    FDA · DeviceZimmer, Inc.Worldwide distribution - US Nationwide including the states of AK, AL, CA, FL,…Official notice →
  4. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a foil pouch with…

    Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.

    FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide in the state of IN and the countries of…Official notice →
  5. US
    Drugs & medicalClass II

    SEASPINE ORTHOPEDICS CORPORATION recalls Mariner RDX Polyaxial Head, REF: MX1-000020; Mariner RDX Extended Polyaxial Head, REF: MX1-000030; Mariner RDX Deformity Head,…

    Screw heads, of pedicle screw systems, have thin lead-in thread that pose a risk of intraoperative cross-threading within the locking cap/screw head interface.

    FDA · DeviceSEASPINE ORTHOPEDICS CORPORATIONUS Nationwide distribution in the states of MI, GA, VA, IN, FL.Official notice →
  6. US
    Drugs & medicalClass II

    Parker Laboratories, Inc. recalls Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

    Product demonstrates low viscosity.

    FDA · DeviceParker Laboratories, Inc.Worldwide distribution - US Nationwide in the states of CA, CO, FL, GA, IL,…Official notice →
  7. US
    Drugs & medicalClass II

    Ion Beam Applications S.A. recalls IBA Proton Therapy System - PROTEUS 235, PTS-10 versions, PTS-11 versions, and PTS-12 versions.

    There is a risk of mistreatment as irradiation is not prevented when some safety parameters are out of tolerance.

    FDA · DeviceIon Beam Applications S.A.US Nationwide distribution in the states of AR, FL, LA, KS, MI, TX, VA.Official notice →
See all drugs & medical recalls →