Advanced Medical Optics, Inc. CeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Posterior Chambet- IOLs (Models:722C, 722Y, 811C, 812C and 812CU) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Posterior Chambet- IOLs (Models:722C, 722Y, 811C, 812C and 812CU)
Brand
Advanced Medical Optics, Inc.
Lot Codes / Batch Numbers
CeeOn¿ One-Piece PMMA 722C, 10 lenses PMMA HSM 722C +19, 5 8094420508 8094430508 8094440508 PMMA HSM 722C +22, 5 8032640508 8032830508 8032840508 8032850508 PMMA HSM 722C +23, 0 8266000508 PMMA HSM 722C +23, 5 8217920508 PMMA HSM 722C +28, 5 8221020508 CeeOn¿ One-Piece PMMA 722Y, 2 lenses PMMA HSM 722Y +29, 0 8136600508 8136610508 CeeOn¿ One-Piece PMMA 811C, 1 lens PMMA HSM 811C +22, 0 8054190508 CeeOn¿ One-Piece PMMA 812CU, 4 lenses PMMA HSM 812CU+17, 5 8139760508 PMMA HSM 812CU+23, 0 8156200508 8156210508 8156220508
Products Sold
CeeOn¿ One-Piece PMMA 722C, 10 lenses PMMA HSM 722C +19,5 8094420508 8094430508 8094440508 PMMA HSM 722C +22,5 8032640508 8032830508 8032840508 8032850508 PMMA HSM 722C +23,0 8266000508 PMMA HSM 722C +23,5 8217920508 PMMA HSM 722C +28,5 8221020508 CeeOn¿ One-Piece PMMA 722Y, 2 lenses PMMA HSM 722Y +29,0 8136600508 8136610508 CeeOn¿ One-Piece PMMA 811C, 1 lens PMMA HSM 811C +22,0 8054190508 CeeOn¿ One-Piece PMMA 812CU, 4 lenses PMMA HSM 812CU+17,5 8139760508 PMMA HSM 812CU+23,0 8156200508 8156210508 8156220508
Advanced Medical Optics, Inc. is recalling CeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Posterior Chambet- IOLs (Models:722C, 722Y, 811C due to A small opening (channel or tunnel) in the seal of the outer Tyvek pouch which contains the lens case, in which the sealed intraocular lens is package. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A small opening (channel or tunnel) in the seal of the outer Tyvek pouch which contains the lens case, in which the sealed intraocular lens is packaged may not be adequately sealed, therefore the potentially compromised outer Tyvek pouch may not be sterile and may potentially contaminate an otherwise sterile field during surgery.
Recommended Action
Per FDA guidance
A product notification letter was mailed to all US domestic customers via overnight carrier (Federal Express) beginning on October 5, 2005. A global notification letter will be translated into the local languages by the international AMO affiliates and mailed to international customers as soon as a listing of all customers is tabulated.
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