Bausch & Lomb, Boston Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lenses, 1 fl. oz. (30 ml)
FDA device recall Z-1735-2009 · posted 2009-08-13 · Terminated
Recall details
- Recalling firm
- Bausch & Lomb Inc
- Reason for recall
- The product failed to meet one of the shelf life specifications at the end of the expiry period.
- Action taken
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- LPN
- Quantity affected
- 56,000 bottles
- Distribution
- Nationwide Distribution.
- Date initiated
- 2009-06-30
- Date posted
- 2009-08-13
- Date terminated
- 2012-05-10
- Location
- Rochester, NY
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| RIGID GAS PERMEABLE CONTACT LENS SOLUTION (K983836) | Polymer Technology Div. Wilmington Partners, L.P. | 1999-02-11 |