Staar Surgical Co Inc STAAR Surgical Intra Occular Lens, Collamer. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
STAAR Surgical Intra Occular Lens, Collamer.
Brand
Staar Surgical Co Inc
Lot Codes / Batch Numbers
All lenses packaged weeks of 9-13 and 23-27 February.
Products Sold
All lenses packaged weeks of 9-13 and 23-27 February.
Staar Surgical Co Inc is recalling STAAR Surgical Intra Occular Lens, Collamer. due to Mislabeled in part. Label set, patient chart labels, and patient ID card serial number did not match the IOL serial number.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mislabeled in part. Label set, patient chart labels, and patient ID card serial number did not match the IOL serial number.
Recommended Action
Per FDA guidance
Consignees are being notified to check their inventory for mismatching labels. Notifications were sent June 17 to all customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026