Westlab Pharmacy recalls Cyclosporine eye drops due to lack of process controls
Westlab Pharmacy recalls Cyclosporine 1% Human Eye Drops (NDC 10002-2776-92) because of lack of process controls. This may affect safety for people with eye conditions.
Recall notice
Lack of Process Controls
Contact the company
What happened, in plain English
Westlab Pharmacy is recalling Cyclosporine 1% Human Eye Drops due to a lack of process controls during manufacturing. This could potentially lead to safety issues for people using the medication for eye conditions. Read more at govinfonow.com/recall/39739-westlab-pharmacy-recalls-cyclosporine-eye-drops-due-to-lack-of.
Source Summary by GovInfoNow · govinfonow.com/recall/39739-westlab-pharmacy-recalls-cyclosporine-eye-drops-due-to-lack-of · Updated October 6, 2026 · FDA enforcement record: FDA #D-0091-2019
Cite this page
“Westlab Pharmacy recalls Cyclosporine eye drops due to lack of process controls.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39739-westlab-pharmacy-recalls-cyclosporine-eye-drops-due-to-lack-of. Based on FDA recall #D-0091-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0091-2019%22&limit=1).
Why it’s dangerous
The recall is due to a lack of process controls during manufacturing, which could result in variations in the medication's quality. This might affect the safety and effectiveness of the eye drops for users.
Who’s affected
People who have purchased or use Cyclosporine 1% Human Eye Drops from Westlab Pharmacy in Gainesville, FL. Those with eye conditions requiring this medication are most at risk.
How to tell if you have this one
Check for the product name 'Cyclosporine 1% Human Eye Drops' with NDC code 10002-2776-92. The lot number is 07262018 and expiration date is 08/25/2018.
- Brand
Westlab Pharmacy- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0089-2019 | Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00; Lot: 03192018@42 Discard after 9/15/2018 | 80 syringes |
| D-0090-2019 | 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; Lot: 06182018@30 Exp. 08/28/2018 | 222 syringes |
| D-0091-2019 | Cyclosporine 1% Human Eye Drops, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-2776-92; Lot: 07262018@7 Exp. 08/25/2018 | 7 droptainers |
What to do — step by step
Check Product Details
Look for the NDC code 10002-2776-92 on the label to confirm if the product is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 21 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0091-2019 (August 10, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0091-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.