Z-0159-2010

Bausch & Lomb ReNu Multi-Purpose Solution, 12 fl.oz. (355 ml), Bausch & Lomb, Incorporated, Rochester, NY...

Name: Z-0159-2010 Bausch & Lomb ReNu Multi-Purpose Solution, 12 fl.oz. (355 ml), Bausch & Lomb, Incorporated, Rochester, NY...
Creator: Bausch & Lomb Inc
Published: 2009-08-17
License: https://open.fda.gov/license/

Bausch & Lomb Incorporated / initiated 2009-08-17 / Terminated

FDA source

Bausch & Lomb Inc began a recall of Bausch & Lomb ReNu Multi-Purpose Solution, 12 fl.oz. (355 ml), Bausch & Lomb, Incorporated, Rochester, NY 14609. Product is used for For the cleaning, rinsing... on 2009-08-17. The reason FDA records is "During routine testing the product failed to meet shelf life specifications". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0159-2010
Status: Terminated
Initiated: 2009-08-17
Posted: 2009-11-10
Terminated: 2012-05-10
Recalling firm: Bausch & Lomb Incorporated
Product: Bausch & Lomb ReNu Multi-Purpose Solution, 12 fl.oz. (355 ml), Bausch & Lomb, Incorporated, Rochester, NY 14609. Product is used for For the cleaning, rinsing, disinfecting, and storage of soft contact lenses.
Product code: LPN Accessories, Soft Lens Products
Reason for recall: During routine testing the product failed to meet shelf life specifications.
FDA root cause: Other
Action: 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.
Quantity in commerce: 5,000 bottles
Distribution: Distribution: Nationwide, Trinidad, St. Croix, St. Thomas, Aruba and Bermuda.
Product codes and lots: Lot Number GA8028.

Product code LPN

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)