Vortex Surgical recalls
4 official recalls and safety alerts involving Vortex Surgical since 2024-02, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Vortex Surgical or the relevant agency.
- 2026-02-11
USVortex Surgical Inc. recalls Vortex Surgical TID Pharos Illuminated Depressor, VS0801B
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FDA · DeviceVortex Surgical Inc.Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL,…Official notice →- US
Vortex Surgical Inc. recalls Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.25GA Convenience Kit - XES…
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.
FDA · DeviceVortex Surgical Inc.Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL,…Official notice → - 2026-01-07
- US
Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
- 2024-02-07
- US
Vortex Surgical Inc. recalls Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps…
FDA · DeviceVortex Surgical Inc.Worldwide - US Nationwide distribution in the states of OH, WA, MN, MI, IA and…Official notice →