← All recalls
Medical Device

Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25

Recall date: 2026-02-11 · Source: FDA_DEVICE
Brand / Firm
Vortex Surgical Inc.
Product
Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25
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
Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25
View official recall notice →