Staar Surgical Co Inc Collamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Collamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF
Brand
Staar Surgical Co Inc
Lot Codes / Batch Numbers
No codes apply
Products Sold
No codes apply
Staar Surgical Co Inc is recalling Collamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF due to Risk of hyperopic refractive changes.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Risk of hyperopic refractive changes.
Recommended Action
Per FDA guidance
Firm is distributing letters to physicians suggesting ways to mitigate the observed contracture of the eye tissues after implantation. Letters will be sent 2/9/2004.
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