Eagle Vision Inc Glaucoma Aqueous Shunt, 209 mm, valved, P/N EG209V Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Glaucoma Aqueous Shunt, 209 mm, valved, P/N EG209V
Brand
Eagle Vision Inc
Lot Codes / Batch Numbers
Serial numbers: 10727A, 10733A, 10734A, 10735A, 10736A, 10737A, 10744A, 10745A, 10746A, 10747A, 10748A, 10749A, 10750A, 10751A, 10794A, 107795A, 10796A, 10797A, 10798A, 10799A, 10806A, 11056A through 11101A, and 11443A through 11456A.
Products Sold
Serial numbers: 10727A, 10733A, 10734A, 10735A, 10736A, 10737A, 10744A, 10745A, 10746A, 10747A, 10748A, 10749A, 10750A, 10751A, 10794A, 107795A, 10796A, 10797A, 10798A, 10799A, 10806A, 11056A through 11101A, and 11443A through 11456A.
Eagle Vision Inc is recalling Glaucoma Aqueous Shunt, 209 mm, valved, P/N EG209V due to Product may have deformed valves which would cause the valve not to operate properly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product may have deformed valves which would cause the valve not to operate properly.
Recommended Action
Per FDA guidance
Written notification of the recall was sent out beginning 04/12/2006 to hospital administrators to advise them of the recall. The letter stated that implanting physicians were to be notified. A second updated notice was sent dated 04/19/2006 which contained more detailed information regarding the product problem.
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