Overview of recall records associated with Arrow International, Inc., Division of Teleflex Medical Inc., including dates, categories and classifications where available.
Classification mix: Class I: 9.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
This page summarizes recall records in which the official source identifies Arrow International, Inc., Division of Teleflex Medical 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.
