Alden Optical recalls

Alden Optical has 13 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 12 Sep 2018. The most frequent reason is sterility.

Total recalls13since 2018

Last 12 months0reported

Class I00% of total

Ongoing0latest 12 Sep 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 11 85%Class III 2 15%

Why alden optical is recalled

Sterility1185%
Other Reasons215%

Product types

Other Medical Devices1185%
Contact Lenses & Eye Devices215%

By year

201813100%

All alden optical recalls, newest first

13 total

Reported	Class	Recall	Company	Reason	Where
12 Sep 2018Device	CLASS III	Zen RC Toric-Gas permeable contact lenses for Daily Wear recalled	Alden Optical	Other	13 states
12 Sep 2018Device	CLASS III	Zenlens Toric-Gas Permeable Contact lenses for Daily Wear recalled	Alden Optical	Other	13 states
21 Mar 2018Device	CLASS II	Astera Multifocal Toric Daily Wear Soft contact recalled	Alden Optical	Sterility	Nationwide
21 Mar 2018Device	CLASS II	Alden HP59 Sphere Daily Wear Soft contact recalled by Alden Optical	Alden Optical	Sterility	Nationwide
21 Mar 2018Device	CLASS II	Alden HP54 Sphere Daily Wear Soft contact recalled by Alden Optical	Alden Optical	Sterility	Nationwide
21 Mar 2018Device	CLASS II	Alden HP54 Toric Daily Wear Soft contact recalled by Alden Optical	Alden Optical	Sterility	Nationwide
21 Mar 2018Device	CLASS II	Alden Classic 55 Toric Daily Wear Soft contact recalled by Alden Optical	Alden Optical	Sterility	Nationwide
21 Mar 2018Device	CLASS II	Alden HP49 Sphere Daily Wear Soft contact recalled by Alden Optical	Alden Optical	Sterility	Nationwide
21 Mar 2018Device	CLASS II	Alden HP49 Toric Daily Wear Soft contact recalled by Alden Optical	Alden Optical	Sterility	Nationwide
21 Mar 2018Device	CLASS II	Alden HP59 Toric Daily Wear Soft contact recalled by Alden Optical	Alden Optical	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.