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Product Recalls & Refunds Online / National

CooperVision, Inc.: Brand Names: MyDay Toric, LensCrafters One Day Premium

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: a limited number of lots were manufactured with an incorrect cylinder power.. Recalled by CooperVision, Inc.. Distribution: Domestic: CA, CO, FL, IL, KY, MI, NC, NE, NJ, NY, OH, OR, UT, VA, WA. International: Australia, Belgium, Canada, Czech Republic, Denmark, France, Germany, Ireland, Italy, Luxembourg, Netherlands, New Zealand, Norway, Poland, Portugal, Spain, Sweden, Switzerland, and United Kingdom.. Classification (Class II — potential health risk). Affected lots/dates: Blister Lot Numbers: (1) 6461501582, (2) 6461501590, (3) 6448502235, (4) 6472500679. Carton Lot numbers: (1) 193465025. Contact the manufacturer or the retailer where you purchased this device to arran

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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