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Vortex Surgical Recalls
15 recalls on record · February 7, 2024 to February 11, 2026 · Medical Devices
Recalls by year
24
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical 25GA Backflush, VS0270.25; 25GA Backflush Retractable, VS0275.27
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical TID Pharos Illuminated Depressor, VS0801B
Hazard: XXX
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Rumex Disposable Diamond Dusted ILM Elevator, 12-7523
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical I2 Injection Kit, VS0500
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Tecfen Retractable Membrane Polisher, QTPR1267-23
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.25
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls 25GA Subretinal Injection Cannula VS0220.25
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive VS0740.23 2. 25GA ACTU8 Forceps Adaptive VS
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4 Illuminated Flex-Tip VK401213 3. 23G Las
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser Probe Curved Cat No. VS0120.25 3.
Hazard: 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.
February 11, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD
Hazard: 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.
January 7, 2026Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Hazard: Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
February 7, 2024Medical DevicesFDA
Vortex Surgical Inc. recalls Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Hazard: 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 Tips occurring in 0.25% of those lots.