Overview of recall records associated with TELEFLEX LLC, including dates, categories and classifications where available.
Classification mix: Class II: 6.
Due to out-of-specification, or potential out-of-specification, levels of endotoxins
Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to…
The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the…
Potential for pilot balloon non-inflation or cuff non-deflation.
Potential for pilot balloon non-inflation or cuff non-deflation.
Potential for pilot balloon non-inflation or cuff non-deflation.
This page summarizes recall records in which the official source identifies TELEFLEX LLC 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.
