Every recall we track for Alcon Research, Ltd. — 16 in all — plus the complaints and injury reports the public filed about them.
Alcon recalls Phaco Standalone Tips (Catalog No. 30KTS, 30RTS) due to potential plastic debris from over-tightening with included wrench, risking patient injury during procedures.
Alcon recalls Custom Pak devices with specific catalog numbers due to potential plastic debris from over-tightening with included wrench. Patients may experience injury during procedures. Check your product's catalog number to see if it's affected.
Alcon recalls Infinity FMS Pak devices with potential plastic debris from over-tightening, causing patient injury during procedures. Check product codes to see if affected.
Alcon recalls Constellation Procedure Pak with catalog numbers 8065750958 and product code 100007216 due to potential plastic debris from over-tightening with included wrench, risking patient injury during procedures.
Alcon recalls Legion FMS Pak devices with potential plastic debris from over-tightening. Affected units include specific catalog numbers and product codes. Stop using immediately to prevent injury during procedures.
Alcon recalls Centurion FMS Pak devices with catalog numbers 8065000133-8065753159 due to potential plastic debris from over-tightening with included wrench, reported to cause patient injury during procedures.
Alcon recalls CyPass Micro-Stent implants due to higher risk of endothelial cell loss in long-term studies. Affected patients should consult their eye doctor for evaluation.
Alcon recalls CyPass Micro-Stent systems due to statistically significant endothelial cell loss in long-term studies. Affected products include specific catalog numbers and lot/serial numbers. Consumers should contact Alcon for details.
Alcon recalls CyPass Micro-Stent devices due to statistically significant endothelial cell loss in long-term studies. Affected patients should consult their eye doctor for evaluation.
Alcon recalls CyPass Micro-Stent devices due to statistically significant endothelial cell loss in long-term studies. Affected units include specific model numbers and lot/serial numbers. No immediate action required per recall details.
Alcon recalls Custom Pak with potential 23GA ULTRAVIT probe included instead of 25GA. Check lot numbers 507492, 507539, 507664 for affected units.
Alcon recalls specific lot (2060953H) of 25+ TOTALPLUS Vitrectomy Paks due to potential inclusion of 23GA ULTRAVIT probe instead of 25GA ULTRAVIT probe.
