Vortex Surgical Inc. recalls 25GA Subretinal Injection Cannula VS0220.25
Recalled Product
25GA Subretinal Injection Cannula VS0220.25
Hazard / Issue
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Pouch UDI 810123480418 Box UDI 810123480692 Lot 2410043
View official government recall
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