FDA Medical Device Recalls (openFDA)
Bausch & Lomb: Bausch & Lomb * ReNu with MoistureLoc, Multi-purpose soft contact lens solution * Sterile * Manufactured by: Bausch & Lomb, Rochester, NY 14609.
- Recall number
- Z-1201-06
- Recalling firm
- Bausch & Lomb
- Product
- Bausch & Lomb * ReNu with MoistureLoc, Multi-purpose soft contact lens solution * Sterile * Manufactured by: Bausch & Lomb, Rochester, NY 14609.
- Status
- Terminated
- Initiated
- 2006-04-13
- Posted
- 2006-08-31
- Terminated
- 2012-09-17
- Reason
- Reports of Fusarium Infections among contact lens wearers.
- Root cause
- Component design/selection
- Action
- Press release was issued 4/13/2006. Letters were sent via blast email to retailers, Pharmacists and Eye Care Practitioners on 04/14/2006.
- Quantity
- 3 million units
- Distribution
- Worldwide, including USA, Latin America, and Asia
- Lot, serial or model codes
- All lots, all sizes
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LPN
- Firm FEI
- 3002749635
- Firm city
- Rochester
- Firm state
- NY
- 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