Overview of recall records associated with AccessClosure, Inc., A Cardinal Health Company, including dates, categories and classifications where available.
Classification mix: Class II: 2.
AccessClosure, Inc. (ACI) is voluntarily recalling the PAXWIRE Occlusion Balloon System device because it was made aware from customers that the device may be removed in the absence of…
A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.
This page summarizes recall records in which the official source identifies AccessClosure, Inc., A Cardinal Health Company 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.
