Alcon Research, Ltd Alcon/Grieshaber Morris ILM Forceps, Direct Action; Manual ophthalmic surgical instrument, Catalog Number: 641.22; Non-sterile/Reusable; Alcon Laboratories, Inc., Fort Worth, TX 76134. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Alcon/Grieshaber Morris ILM Forceps, Direct Action; Manual ophthalmic surgical instrument, Catalog Number: 641.22; Non-sterile/Reusable; Alcon Laboratories, Inc., Fort Worth, TX 76134.
Brand
Alcon Research, Ltd
Lot Codes / Batch Numbers
Lot Numbers: F58834, F60464, F60465 and F60466.
Products Sold
Lot Numbers: F58834, F60464, F60465 and F60466.
Alcon Research, Ltd is recalling Alcon/Grieshaber Morris ILM Forceps, Direct Action; Manual ophthalmic surgical instrument, Catalog N due to Device corrosion: Forceps are prone to corrosion and possibly premature fracture and/or malfunction.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Device corrosion: Forceps are prone to corrosion and possibly premature fracture and/or malfunction.
Recommended Action
Per FDA guidance
Consignees were notified by an Urgent Medical Device Recall that was sent via fax on 03/07/08. Users were instructed to cease using the affected products and to return a Recall Acknowledgement Form to the recalling firm. The sales representative will pick up the affected product and discuss replacement alternatives. For additional information, contact 1-800-757-9780.
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 noticePage updated: Jan 10, 2026