Alcon Research, Ltd. recalls

35 recalls on record · latest: June 28, 2023

Official U.S. recall history for Alcon Research, Ltd., compiled from official government records.

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Alcon Research, LTD. recalls Centurion FMS Pak

June 28, 2023 · Medical device recalls Moderate risk Reports of patient injury during use in procedures due to potential for plastic…

Alcon Research, LTD. recalls Legion FMS Pak

June 28, 2023 · Medical device recalls Moderate risk Reports of patient injury during use in procedures due to potential for plastic…

Alcon Research, LTD. recalls Constellation Procedure Pak

June 28, 2023 · Medical device recalls Moderate risk Reports of patient injury during use in procedures due to potential for plastic…

Alcon Research, LTD. recalls Infinity FMS Pak

June 28, 2023 · Medical device recalls Moderate risk Reports of patient injury during use in procedures due to potential for plastic…

Alcon Research, LTD. recalls Alcon Custom Pak

June 28, 2023 · Medical device recalls Moderate risk Reports of patient injury during use in procedures due to potential for plastic…

Alcon Research, LTD. recalls Phaco Standalone Tips

June 28, 2023 · Medical device recalls Moderate risk Reports of patient injury during use in procedures due to potential for plastic…

Alcon Research, LTD. recalls CyPass System 241-S, CYPASS MICRO-STENT, CYPASS LOADED, CYPASS APPLIER, REF CATALOG #: 8065754003 For ophthalmic use.

August 28, 2018 · Medical device recalls High risk Analysis of the completed dataset from the COMPASS-XT long-term study showed th…

Alcon Research, LTD. recalls CyPass System 241, Intraocular Pressure Lowering Implant, CYPASS MICRO-STENT, CYPASS APPLIER, REF: 8065754001. For opht…

August 28, 2018 · Medical device recalls High risk Analysis of the completed dataset from the COMPASS-XT long-term study showed th…

Alcon Research, LTD. recalls CyPass ULTRA SYSTEM, CYPASS MICRO-STENT, CYPASS APPLIER, REF CATALOG #: 8065754007. For ophthalmic use.

August 28, 2018 · Medical device recalls High risk Analysis of the completed dataset from the COMPASS-XT long-term study showed th…

Alcon Research, LTD. recalls CyPass System 241, Intraocular Pressure Lowering Implant, CYPASS MICRO-STENT, CYPASS APPLIER, REF: 8065754010. For opht…

August 28, 2018 · Medical device recalls High risk Analysis of the completed dataset from the COMPASS-XT long-term study showed th…

Alcon Research, LTD. recalls Alcon 25+¿ TOT ALPLUS¿ Vitrectomv Pak Includes all necessary items for a core vitrectomy procedure and connects to the…

January 12, 2018 · Medical device recalls Moderate risk Alcon is conducting this Voluntary Medical Device Recall for a specific lot (20…

Alcon Research, LTD. recalls Custom Pak¿ (Custom Pak in which Alcon 25+¿ TOTALPLUS¿ Vitrectomy Pak is a component.) Includes all necessary items for…

January 12, 2018 · Medical device recalls Moderate risk Alcon is conducting this Voluntary Medical Device Recall for a specific lot (20…

Alcon Research, LTD. recalls Alcon Custom Pak

August 8, 2017 · Medical device recalls Moderate risk Alcon is initiating a medical device recall, after receiving notification from…

Alcon Research, Ltd. recalls ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery

June 30, 2017 · Medical device recalls Moderate risk Some ORA Carts have the potential to return an incorrect IOL power measurement…

Alcon Research, Ltd. recalls ORA System with VerifEye, Catalog Number 8065998300 For use during intraocular lens surgery

June 30, 2017 · Medical device recalls Moderate risk Some ORA Carts have the potential to return an incorrect IOL power measurement…

Alcon Research, Ltd. recalls LX3 Floor Stand for LuxOR Ophthalmic Microscope; Endure LuxOR Q-VUE Ophthalmic Microscope. LX3 Microscope Floor Stands…

May 25, 2017 · Medical device recalls Moderate risk Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope may…

Alcon Research, Ltd. recalls Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessorie…

March 27, 2017 · Medical device recalls Moderate risk Alcon is initiating a Voluntary Medical Device Removal because the product supp…

Alcon Research, Ltd. recalls Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following c…

September 5, 2016 · Medical device recalls Moderate risk The intraocular lens could become lodged within the cartridge

Alcon Research, Ltd. recalls Alcon AcrySof IQ IOL with ULTRASERT Delivery System Product Usage: The Alcon AcrySof IQ Intraocular Lens (IOL) is an ac…

July 28, 2016 · Medical device recalls Moderate risk The ULTRASERT Delivery System from certain lots have an inferior surface charac…

Alcon Research, Ltd. recalls LAUREATE World Phaco System

July 28, 2016 · Medical device recalls Moderate risk Steps 16-25 are missing from the LAUREATE Multipak FMS Directions for Use (DFU)

Alcon Research, Ltd. recalls CENTURION Vision System

May 24, 2016 · Medical device recalls Moderate risk The grounding pin within the Power Entry Switch on certain systems was suscepti…

Alcon Research product recalled over mold contamination

April 28, 2016 · Medical device recalls Moderate risk Alcon is conducting this Voluntary Medical Device Removal for specific lots of…

Alcon Research, Ltd. recalls LenSx Laser System. Indicated for use in patients undergoing cataract surgery and refractive surgery.

April 14, 2016 · Medical device recalls Moderate risk Alcon is conducting a voluntary recall of all LenSx Lasers with Corneal Flap Ca…

Alcon Research, Ltd. recalls VERION Reference Unit (Vision Planner) Product Usage: The VERION Image Guided system is an advanced surgical planning,…

March 1, 2016 · Medical device recalls Moderate risk Alcon is conducting a voluntary medical device correction of all VERION Referen…

TEARS Naturale FREE lubricant eye drops recalled over sterility concerns

February 9, 2016 · Drug & medication recalls Moderate risk Lack of Assurance of Sterility: Some single-use vials may be filled with water…

Alcon Research, Ltd. recalls Expansion of previous recall of AcrySof IQ ReSTOR and AcrySof IQ ReSTOR Toric IOL; now to include AcrySof IQ Toric mode…

September 29, 2015 · Medical device recalls High risk Continued increase in reports of post-operative inflammation in patients who re…

Alcon Research, Ltd. recalls Custom Pak 9319-27. Single-use medical devices and accessories designed by medical professionals for a specific ophthal…

September 21, 2015 · Medical device recalls Moderate risk The recalled lot of custom paks are labeled as latex free and contain latex glo…

Alcon Research, Ltd. recalls LX3 Floor Stand for Endure Luxite Envision Optical System; Endure LuxOR Q-Vue. Product Usage: The LX3 Microscope Floor…

August 11, 2015 · Medical device recalls Moderate risk Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands after…

Alcon Research, Ltd. recalls 23G and 25G Constellation Totalplus Paks provides access into the posterior segment of the eye for surgical instruments…

August 11, 2015 · Medical device recalls Moderate risk The product has potential to leak beyond their design specification.

Alcon Research, Ltd. recalls Custom Paks containing 23G and 25G valved trocar cannula provide access into the posterior segment of the eye for surgi…

August 11, 2015 · Medical device recalls Moderate risk The product has potential to leak beyond their design specification.

Alcon Research, Ltd. recalls Alcon 23G and 25G Valved Entry System provides access into the posterior segment of the eye for surgical instruments wi…

August 11, 2015 · Medical device recalls Moderate risk The product has potential to leak beyond their design specification.

Alcon Research, Ltd. recalls Accurus 2500 Standalone Vitreous Probe REF 8065741018; Accurus 23 GA Standalone Vitreous Probe REF 8065750821; Accurus…

June 2, 2015 · Medical device recalls Moderate risk Insufficient seal on the outside packaging, potentially affecting the sterility…

Alcon Research, Ltd. recalls The Alcon Custom Pak. The Alcon Customer Pak is an assemblage of single-use medical devices and accessories designed by…

April 28, 2015 · Medical device recalls Moderate risk The supplier of the Devon Light Glove, a component of the Alcon Custom PAK, rec…

Alcon Research, Ltd. recalls ReSTOR intraocular lens and ReSTOR Toric intraocular lens. The Alcon AcrySof IQ ReSTOR and IQ ReSTOR Toric intraocular…

April 15, 2015 · Medical device recalls High risk There are reports of post - operative inflammation and/or toxic anterior segmen…

Alcon Research, Ltd. recalls INFINITI Ultrasound Pack. Catalog Numbers: 8065751716, 8065751717, 8065751718, 8065751720, 8065751721, 8065751723. An o…

October 6, 2014 · Medical device recalls Moderate risk The recalling firm received complaints related to leakage from the tubing near…