Overview of recall records associated with Teleflex, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 10, Class I: 1.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Teleflex Medical has issued an advisory notification for the RUSCH Curved Reinforced Endotracheal Tube because of a discrepancy between the labeled cuff diameter and the actual cuff…
Connector mount cracks which may lead to a leak failure during use and necessitate immediate replacement in the breathing circuit. If leak exists and is left untreated, patient may be…
This page summarizes recall records in which the official source identifies Teleflex, Inc. 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.
