Bausch & Lomb Incorporated Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box.
Brand
Bausch & Lomb Incorporated
Lot Codes / Batch Numbers
Julian date coded ''2003163''
Products Sold
Julian date coded ''2003163''
Bausch & Lomb Incorporated is recalling Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manufact due to The firm's DP8200 Microflow Needle Packs were labeled with the firm's DP8115 Phaco Needle Packs and visa versa.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm's DP8200 Microflow Needle Packs were labeled with the firm's DP8115 Phaco Needle Packs and visa versa.
Recommended Action
Per FDA guidance
Firm notified customers by phone and letter 8/25/2003 and advised of needle mix-up. Customers were requested to quarantine affected product and return product with response form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
FL, IL, IN, IA, MA, WI
Page updated: Jan 10, 2026