Bausch & Lomb ReNu Multi-Purpose Solution, 12 fl.oz. (355 ml), Bausch & Lomb, Incorporated, Rochester, NY 14609. Product
FDA device recall Z-0159-2010 · posted 2009-11-10 · Terminated
Recall details
- Recalling firm
- Bausch & Lomb Inc
- Reason for recall
- During routine testing the product failed to meet shelf life specifications.
- Action taken
- Consignees were notified by letter on/about August 17, 2009. All consignees were asked to review their inventory and return any of the affected product to Stericycle Pharmaceutical Services. For questions about the recall process or need additional shipping labels, please contact Stericycle Inc. at 1-888-345-83 16. For questions regarding this recall, please contact Bausch & Lomb's Customer Resource Center at 1-800-828-6974.
- Root cause
- Other
- Status
- Terminated
- Product code
- LPN
- Quantity affected
- 5,000 bottles
- Distribution
- Distribution: Nationwide, Trinidad, St. Croix, St. Thomas, Aruba and Bermuda.
- Date initiated
- 2009-08-17
- Date posted
- 2009-11-10
- Date terminated
- 2012-05-10
- Location
- Rochester, NY
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