FDA recall record

Acumedia Manufacturers Sabouraud Dextrose Agar w /Lecithin and Tween 20 Acumedia PN 91081 recall — FDA Z-2212-2017

Storage temperature listed on the label was incorrect. Label stated 2-30¿C. Actual storage temperature is 2-8¿C.

Class IIIclassification
Z-2212-2017official record ID
Jun 7, 2017report date

Recall record at a glance

Official recordZ-2212-2017
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAcumedia Manufacturers, Inc.
Report dateJun 7, 2017
Recall initiation dateAug 8, 2016
Quantity10 units
LocationLansing, MI, United States

Official product description

Sabouraud Dextrose Agar w /Lecithin and Tween 20 Acumedia PN 91081 Product Usage: Used for the isolation of fungi from surfaces sanitized with quaternary ammonium compounds

Why the product was recalled

Storage temperature listed on the label was incorrect. Label stated 2-30¿C. Actual storage temperature is 2-8¿C.

Distribution information

US in the state of IL

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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