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U.S. Department of Health and Human Services

Class 2 Device Recall

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 Class 2 Device Recallsee related information
Date Initiated by FirmOctober 05, 2005
Date PostedOctober 28, 2005
Recall Status1 Terminated 3 on May 23, 2008
Recall NumberZ-0096-06
Recall Event ID 33849
PMA NumberP960034 
Product Classification Intraocular Lens - Product Code HQL
ProductCeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Posterior Chambet- IOLs (Models:722C, 722Y, 811C, 812C and 812CU)
Code Information 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      
Recalling Firm/
Manufacturer		 Advanced Medical Optics, Inc.
1700 E Saint Andrew Pl
Santa Ana CA 92705-4933
For Additional Information ContactSandra F. Selvaggi
714-247-8656
Manufacturer Reason
for Recall		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.
FDA Determined
Cause 2		Other
ActionA 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.
Quantity in Commerce45 (4 in US)
DistributionNationwide, Austria, Belgium, Switzerland, Germany, Denmark, France, UK, Guadelope, Hong Kong, Croatia, India, Italy, Netherlands, and Vietnam
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
PMA DatabasePMAs with Product Code = HQL
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