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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K042242
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Alden HP59 Toric Daily Wear Soft contact; Catalog Number: AOHPT59 Product Usage: The ALDEN TORIC... 2 03/13/2018 Alden Optical
Alden HP59 Sphere Daily Wear Soft contact; Catalog Number: AOHPS59 Product Usage: The ALDEN SPHE... 2 03/13/2018 Alden Optical
Alden Classic 55 Toric Daily Wear Soft contact; Catalog Number: AOCLT55 Product Usage: The ALDEN... 2 03/13/2018 Alden Optical
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