Overview of recall records associated with Alcon Research, Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 9, Class I: 4.
Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial cell loss (ECL) compared to…
Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial cell loss (ECL) compared to…
Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial cell loss (ECL) compared to…
Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial cell loss (ECL) compared to…
Alcon is conducting this Voluntary Medical Device Recall for a specific lot (2060953H) of its 25+ TOTALPLUS Vitrectomy Pak due a potential that a 23GA ULTRAVIT probe may be included within…
Alcon is conducting this Voluntary Medical Device Recall for a specific lot (2060953H) of its 25+ TOTALPLUS Vitrectomy Pak due a potential that a 23GA ULTRAVIT probe may be included within…
Lack of Assurance of Sterility: Some single-use vials may be filled with water rather than the product solution and the firm cannot guarantee the sterility of the water-filled vials.
This page summarizes recall records in which the official source identifies Alcon Research, Ltd. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
