Medical Device

25GA Subretinal Injection Cannula VS0220.25

Recall date: 2026-02-11 · Source: FDA_DEVICE

Brand / Firm

Product

Reason for recall

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.

Units affected

14,789 (8651 US; 6138 OUS)

Description

25GA Subretinal Injection Cannula VS0220.25

View official recall notice →