No image published for this recall
An official FDA notice concerns Alcon Research - safety alert. An official FDA notice concerns Alcon Research. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-11-05. Lots: A8041128. Recall numbers: Z-0326-2026. Check the official notice for the complete list. Published 2025-11-05.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
82
Recall number
Z-0326-2026
Official notice
2025-11-05
The hazard
The hazard
An official FDA notice concerns Alcon Research. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-11-05. Lots: A8041128. Recall numbers: Z-0326-2026. Check the official notice for the complete list.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Lots
Event Ids
Recall Numbers
Checked manually this time?
The app alerts you when a new official recall is published — no searching, no checking back.
Turn on recall alertsWhere it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Affected area 2
Company & contacts
Company & contacts
Brand: Alcon Research. Contact: Alcon Research LLC.
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Units affected
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
View full official noticeRelated recalls
a product listed in the official notice - safety alert
16 Jul 2025a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
Constellation Procedure Pak - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery - safety alert
Weekly recall digest
Get next week's recalls before you need them.
One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.
The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.
This recall was published 5 Nov 2025. The next one won't wait for you to search.
RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.
