FDA Medical Device Recalls (openFDA)
Advanced Medical Optics, Inc.: Tecnis Multifocal Silicone Posterior Chamber IOLs (Model: ZM900)
- Recall number
- Z-0094-06
- Recalling firm
- Advanced Medical Optics, Inc.
- Product
- Tecnis Multifocal Silicone Posterior Chamber IOLs (Model: ZM900)
- Status
- Terminated
- Initiated
- 2005-10-05
- Posted
- 2005-10-28
- Terminated
- 2008-05-23
- Reason
- 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.
- Root cause
- Other
- Action
- 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.
- Quantity
- 7 (none in US)
- Distribution
- Nationwide, Austria, Belgium, Switzerland, Germany, Denmark, France, UK, Guadelope, Hong Kong, Croatia, India, Italy, Netherlands, and Vietnam
- Lot, serial or model codes
- Tecnis¿ Silicone ZM900, 7 lenses Tecnis Multi 12mm ZM900+23,0 8027950508 8027960508 8027990508 Tecnis Multi 12mm ZM900+24,0 8026240508 8026260508 8026280508 8026310508
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- HQL
- Firm FEI
- 3003843509
- Firm city
- Santa Ana
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28