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…

Read the official notice →
Date
2024-04-03
Country
United States
Brand
Alcon Research
Product
SYRINGE,BULB,2OZ/60CC,GREEN, Part: 300055070, packaged inside Alcon Custom-Pak Surgical Procedure Packs, Products: 18018-06, 3865-44,…
Classification
Class II
Units
US Nationwide distribution in the states of OH, WV.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2024-07-24
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    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 →
  3. 2024-06-05
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    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 →
  5. 2024-05-01
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    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.

    FDA · DeviceAlcon Research, LLCWorldwide distribution - U.S. Nationwide including in the states of AK, AR,…Official notice →
  7. 2023-11-15
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    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 →
  9. 2023-10-18
  10. US
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    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 →
  11. 2023-08-23
  12. US
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    Alcon Research, LTD. recalls Centurion FMS Pak

    Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

    FDA · DeviceAlcon Research, LTD.Worldwide distribution - US Nationwide and the countries of Aland Islands,…Official notice →
All 22 Alcon Research recalls →

Other drugs & medical recalls in the United States

  1. 2024-04-03
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    Boston Scientific Corporation recalls Obsidio Conformable Embolic, Material Numbers (UPN): a) M0013972001010, b) M0013972101010

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    FDA · DeviceBoston Scientific CorporationUSOfficial notice →
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    Ortho-Clinical Diagnostics recalls VITROS Performance Verifier I

    The issue was mismatched diluent lots assembled into VITRO Chemistry Products Performance Verifier I and II. This issue has the potential to cause erroneous Quality Control (QC) results that could lead to testing…

    FDA · DeviceOrtho-Clinical DiagnosticsWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →
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    Hologic, Inc. recalls Aptima CMV Quant Assay, Reference numbers: AW-22600-001, AW-25509-001, and AW-26381-001 Amplification Reagent, Enzyme Reagent, Promoter…

    Use of assay along with plasma specimen may result in error code which would invalidate sample.

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    Olympus Corporation of the Americas recalls InstaClear Lens Cleaner-indicated for use during routine diagnostic procedures and during endoscopic sinus surgery. Model…

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    Bruder Healthcare Company, LLC recalls Thermalon Stye Compress, Item Number 24352

    Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

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See all drugs & medical recalls →