US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 10, 2018 (8 years ago)

ADAA Cataract Drops, (Lido 1.47%, Phenyleph 0.294% Cyclopentolate 0.147%, Tropicamide…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Process Controls

What was recalled

ADAA Cataract Drops, (Lido 1.47%, Phenyleph 0.294% Cyclopentolate 0.147%, Tropicamide 0.0735%, Moxiflox 0.0294%, Ketorolac 0.0147%) 1x 1cc syringe, Westlab Pharmacy, Inc., Gainesville, FL 32607 --- NDC 10002-2579-05

Recalling firm
Westlab Pharmacy, Inc. dba Westlab Pharmacy
NDC code
10002-2579-05
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0090-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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