Overview of recall records associated with Teleflex Medical Europe Ltd, including dates, categories and classifications where available.
Classification mix: Class II: 11.
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized.
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
These one-way valves may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient.
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic…
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic…
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic…
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic…
This page summarizes recall records in which the official source identifies Teleflex Medical Europe 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.
