C.R. Bard Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box, each recall — FDA Z-1309-2018
Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
Overview of recall records associated with C.R. Bard, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 45, Class I: 5.
Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
This page summarizes recall records in which the official source identifies C.R. Bard, 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.