Z-1735-2009

Bausch & Lomb, Boston Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lenses, 1 fl...

Name: Z-1735-2009 Bausch & Lomb, Boston Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lenses, 1 fl...
Creator: Bausch & Lomb Inc
Published: 2009-06-30
License: https://open.fda.gov/license/

Bausch & Lomb Incorporated / initiated 2009-06-30 / Terminated

FDA source

Bausch & Lomb Inc began a recall of Bausch & Lomb, Boston Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lenses, 1 fl. oz. (30 ml), Bausch & Lomb Incorporated... on 2009-06-30. The reason FDA records is "The product failed to meet one of the shelf life specifications at the end of the expiry period". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1735-2009
Status: Terminated
Initiated: 2009-06-30
Posted: 2009-08-13
Terminated: 2012-05-10
Recalling firm: Bausch & Lomb Incorporated
Product: Bausch & Lomb, Boston Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lenses, 1 fl. oz. (30 ml), Bausch & Lomb Incorporated, Rochester, NY 14609.
Product code: LPN Accessories, Soft Lens Products
Reason for recall: The product failed to meet one of the shelf life specifications at the end of the expiry period.
FDA root cause: Other
Action: Bausch & Lomb issued an "Urgent Voluntary Medical Device Recall" notice dated June 26, 2009. All consignees were requested to review their inventory, and return any of the affected product to Stericycle Pharmaceutical Services, Indianapolis, IN. A Business Reply Card was included to be returned to Bausch & Lomb via US mail. A prepaid UPS Packing Slip was also provided to return the affected product. For further questions, contact Bausch & Lomb Customer Resource Center at 1-800-828-9030.
Quantity in commerce: 56,000 bottles
Distribution: Nationwide Distribution.
Product codes and lots: Lot Number: GA7060; Item Number: 7474G. Expires January 2009.

Product code LPN

K983836Class IIRigid Gas Permeable Contact Lens SolutionPolymer Technology Div. Wilmington Partners, L.P. / cleared 1999-02-11

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 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)