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Dutch Ophthalmic USA, Inc. recalls The device is a 25-gauge infusion line that is part of 25-gauge surgical pack labeled TDC Vitrectomy Pack VGPC 25g , Pr
Recalled August 18, 2021 · FDA recall Z-2252-2021 · Dutch Ophthalmic USA
Hazard
Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing 23-gauge infusion line · FDA Class II
Units
16 boxes
Sold at
US Nationwide Distribution in the states of AL, CA, CO, FL, MI
Description
Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing 23-gauge infusion line
Product
The device is a 25-gauge infusion line that is part of 25-gauge surgical pack labeled TDC Vitrectomy Pack VGPC 25g , Product Number 8525.201.
Manufacturer(s)
Dutch Ophthalmic USA, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →