Data Foundry

Medical device recalls 2018

Zen RC Toric-Gas permeable contact lenses for Daily Wear in a 10-cc… — Class III medical device recall Z-2982-2018

Terminated recall by Alden Optical, reported 2018-09-12, distributed in CA, GA, IL, MD, NC, NJ, NV, OH…. Vials labeled for the prescriptions contained incorrect lenses

Recall numberZ-2982-2018
Product typeMedical device
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAlden Optical, Lancaster, NY, United States
Recall initiated2018-07-03
Classified2018-09-06
Reported by FDA2018-09-12
Terminated2020-02-28
DistributedCA, GA, IL, MD, NC, NJ, NV, OH, OK, PA, TN, TX, UT
Quantity4 vials
Reason classeslabeling
UPC / GTIN / UDI-DI00785811435660

Product

Zen RC Toric-Gas permeable contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx)as follows: Zen RC TPC (Toric Peripheral Curve) Zen RC FT (Front Toric Optics) Catalog Number: AOZNT Zenlens Toric - Zenlens contact lenses are indicated for daily wear for the correction of refractive arnetropia (myopia, hyperopia, and astigmatism) in aphakic and nonaphakic persons with non-diseased eyes.

Reason for recall

Vials labeled for the prescriptions contained incorrect lenses

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2982-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.