Overview of recall records associated with Medical Action Industries, Inc. 306, including dates, categories and classifications where available.
Classification mix: Class II: 10, Class I: 4.
Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's…
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood…
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches…
The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
This page summarizes recall records in which the official source identifies Medical Action Industries, Inc. 306 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.
