Friday, June 25, 2021

Avid Medical Recalls Convenience Kits for Fungal Contamination Risk

Serious injuries or death may result from the use of these devices. The FDA has identified this as a Class I recall, the most serious type.

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FDA - Center for Devices and Radiological Health

Avid Medical Recalls Medical Convenience Kits for Risk of Fungal Contamination

Avid Medical is recalling medical convenience kits that include a "3mL Chloraprep Applicator" were distributed from May 9, 2019 to March 19, 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.

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Questions?

If you have questions about this recall, contact the Division of Industry and Consumer Education.


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