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Contact Lenses & Vision

AllImplants & Prosthetics(225)Monitoring Devices(272)Diagnostic Equipment(819)Home Healthcare(232)Contact Lenses & Vision(17)Surgical Equipment(890)

17 recalls

per page
MSM Nutraceuticals
Medium RiskFDA Drug

MSM Nutraceuticals, LLC: Various MSM Eye Drops Recalled for Lack of Sterility

  • Distributed nationwide
  • Sold at Dr. Berne's Whole Health Products, Retailers nationwide
Recalled
Added
Altaire Pharmaceuticals
High RiskFDA Drug

Altaire Pharmaceuticals, Inc.: Various Ophthalmic Ointments and Drops Recalled for Lack of Sterility

  • Distributed nationwide
  • Sold at Walmart, CVS Pharmacy +2 more
  • Unspecified microorganisms (lack of sterility assurance) contamination
Recalled
Added
Medium RiskFDA Device

TECNIS Eyhance IOL Recalled for Lens Unfolding Issues

  • Sold in 11 states
  • Sold at Authorized medical distributors, Surgical centers
Recalled
Added
Medium RiskFDA Device

Johnson & Johnson Surgical Vision, Inc.: TECNIS Toric II OptiBlue IOL Recalled for Misaligned Axis Marks

  • Sold at International distributors in Japan
Recalled
Added
Medium RiskFDA Device

ACUVUE OASYS MAX 1-Day MULTIFOCAL Contact Lenses Recalled for Defects

  • Sold in 32 states
  • Sold at Eye care professionals, Optical retailers +1 more
  • 114,165 units affected
Recalled
Added
CooperVision
Medium RiskFDA Device

MyDay Toric and Other Contact Lenses Recalled for Incorrect Cylinder Power

  • Sold in 15 states
  • Sold at LensCrafters, Pearle Vision +4 more
  • 33,990 units affected
Recalled
Added
CooperVision
Medium RiskFDA Device

MyDay, Sofmed, and Voyant Contact Lenses Recalled for Sterilization Issue

  • Sold in 4 states
  • Sold at Optometrists, Ophthalmologists +1 more
  • Invalid sterilization cycle contamination
Recalled
Added
Contamac Solutions
Medium RiskFDA Device

Nutrifill Contact Lens Insertion Solution Recalled for Lack of Sterility

  • Sold in 25 states
  • Sold at Eye care professionals, Specialized distributors
  • Non-sterile contamination
Recalled
Added
CooperVision
Medium RiskFDA Device

CooperVision, Inc.: Biofinity Soft Contact Lenses Recalled Due to Incorrect Prescription Power

  • Distributed nationwide
  • Sold at Eye care professionals, authorized distributors
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon Research LLC: Contact Lenses Recalled for Quality and Vision Performance Issues

  • Sold in 51 states
  • Sold at eye care professionals, authorized optical retailers
  • 92,835 units affected
Recalled
Added
Bausch & Lomb Surgical
Low RiskFDA Device

Bausch & Lomb Akreos Intraocular Lenses Recalled for Diopter Power Error

  • Sold in Arizona, California
  • Sold at surgical centers, hospitals +1 more
Recalled
Added
PARAGON VISION SCIENCES
Medium RiskFDA Device

PARAGON VISION SCIENCES, Inc: ISee and Fargo Ortho-K Lenses Recalled for Lack of FDA Approval

  • Sold in 51 states
  • Sold at Eye care professionals, Optometrists +1 more
  • 102,362 units affected
Recalled
Added
CooperVision
Medium RiskFDA Device

Biofinity XR and Multifocal Contact Lenses Recalled for Sterility Risk

  • Distributed nationwide
  • Sold at Eye care professionals, Optical retailers +1 more
  • Microbial contamination risk due to loss of sterility contamination
Recalled
Added
Ontact
Medium RiskFDA Device

Ontact Inc: 24K Premium Lense Contact Lenses Recalled for Potential Bacterial Contamination

  • Sold in California, Nevada
  • Sold at Updream Inc.
  • Bacteria contamination
Recalled
Added
Boston Foundation For Sight
Medium RiskFDA Device

BostonSight SCLERAL and PROSE Lenses Recalled for Manufacturing Errors

  • Distributed nationwide
  • Sold at Eye care providers, Specialty clinics
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon PRECISION1 One-Day Contact Lenses Recalled for Weak Seal and Sterility Risk

  • Sold in 19 states
  • Sold at Authorized eye care providers
Recalled
Added
Enchroma
Medium RiskFDA Device

Enchroma Inc: EnChroma Safety Glasses Recalled for Failing High Impact Safety Standards

  • Sold in 24 states
  • Sold at Enchroma Inc
Recalled
Added