A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: CooperVision Avaira (enfilcon A) Sphere Soft Contact Lens: Class 1 Recall – Unintended Residue on Lenses. According to the Food & Drug Administration FDA’s MedWatch:
Symptoms may range from hazy, blurry vision, discomfort to eye injuries requiring medical treatment.
For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: CooperVision Avaira (enfilcon A) Sphere Soft Contact Lens: Class 1 Recall – Unintended Residue on Lenses.
To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.
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