Every recall we track for Vortex Surgical Inc. — 15 in all — plus the complaints and injury reports the public filed about them.
Vortex Surgical recalls Lindsell Sutured IOL Marker (VS0390) due to potential voids in Tyvek pouch seals that could cause infection. Affected units have specific catalog numbers and lots.
Vortex Surgical recalls Rumex Disposable Diamond Dusted ILM Elevator model 12-7523 due to potential voids in Tyvek pouch seals that could cause infection. Affected units have specific catalog numbers and lots.
Vortex Surgical recalls two types of single-use vitrectomy lenses due to potential voids in Tyvek pouch seals that could cause infection. Affected items include specific catalog numbers and lots sold in 2024.
Vortex Surgical Inc. recalls specific disposable surgical forceps and cannulas due to potential voids in Tyvek pouch seals that could cause infection. Affected items include models VS0740.23, VS0740.25, and others with specific UDI and lot numbers.
Vortex Surgical recalls 25GA Subretinal Injection Cannula VS0220.25 with potential infection risk due to compromised sterile packaging. Affected units include specific catalog numbers and lots.
Vortex Surgical recalls Tecfen Retractable Membrane Polisher model QTPR1267-23 due to potential voids in Tyvek pouch seals that could cause infection. Affected units have specific catalog numbers and lots.
Vortex Surgical recalls 25GA I.D.D. Internal Delivery Device with potential voids in Tyvek pouch seals, risking infection. Affected units have specific catalog numbers and lots.
Oertli 23G Laser Probes with specific model numbers and lots may have seal voids causing infection risk. Affected units include OS4 Flex-Tip and Illuminated Flex-Tip probes with catalog numbers VK401113, VK401213, etc. Contact for replacement or return.
Vortex Surgical recalls 25GA Backflush pouches with specific model numbers and lots due to potential seal voids causing infection risk. Affected items may need replacement to prevent contamination.
Vortex Surgical recalls I2 Injection Kit VS050: Voids in Tyvek pouch seals may cause infection. Affected units have specific catalog numbers and lots. Stop using immediately to prevent contamination.
Vortex Surgical recalls VS0801B Illuminated Depressor due to potential injury risk. Affected units have specific UDI codes. Stop using immediately to avoid injury.
Vortex Surgical recalls specific laser probe models due to potential voids in sterile pouch seals, risking infection. Affected units include 23GA and 25GA curved and straight probes with certain catalog numbers and lots.
Vortex Surgical recalls 25GA Convenience Kits with specific model numbers and lots due to potential voids in Tyvek pouch seals that could cause infection. Affected kits include FNX, FXX, and XES models with certain lot numbers.
Vortex Surgical recalls 25ga Illuminated Flex-Tip Laser Probes with specific UDI codes due to potential failure to pass through 25ga cannulas smoothly. Affected units may not function correctly during surgical procedures.
Vortex Surgical recalls ACTU8 Forceps with residue risk in 0.25% of lots. Affected units have specific lot numbers and model. Consumers should check their product details to determine if recalled.
