MAI Recalls Medical Convenience Kits for Risk of Fungal Contamination

Learn more about MAI's recall of convenience kits due to risk of fungal contamination.

If your email program has trouble displaying this email, view as a webpage. Medical Action Industries, Inc. 306 Recalls Medical Convenience Kits for Risk of Fungal (Aspergillus Penicillioides) Contamination Medical Action Industries' is recalling the Medical Convenience Kits that include a "3mL Chloraprep Applicator" that were distributed from December 12, 2019 to March 22, 2021. The Chloraprep is manufactured by BD/Carefusion and was recalled due to the risk of contamination with a specific type of fungus called Aspergillus penicillioides. The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Read More Questions? If you have questions about this recall, contact the Division of Industry and Consumer Education (DICE).

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