FDA recall record

Leiter's Compounding Mitomycin 0.02% (0.2 mg/mL) in Sterile Water for Injection (Injection) recall — FDA D-0015-2017

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIclassification
D-0015-2017official record ID
Oct 19, 2016report date

Recall record at a glance

Official recordD-0015-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLeiter's Compounding
Report dateOct 19, 2016
Recall initiation dateSep 20, 2016
Quantity76,315 total units, all products
LocationSan Jose, CA, United States

Official product description

Mitomycin 0.02% (0.2 mg/mL) in Sterile Water for Injection (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-005-35

Why the product was recalled

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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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