FDAJanuary 13, 2017drug

Duopa (carbidopa and levodopa enteral suspension), 4.63 mg/20 mg per mL, 100 mL cassette, 7 cassettes per carton, Rx Only, AbbVie Inc., North Chicago, IL 60064 --- NDC 0074-3012-07

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Stability Specifications: confirmed out of specification results obtained during refrigerated material stability testing indicating that drug may settle within drug cassettes nearing the end of their refrigerated shelf-life

What to do

FDA enforcement status: Terminated

Brands named

abbvie

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Duopa (carbidopa and levodopa enteral suspension), 4.63 mg/20 mg per mL, 100 mL cassette, 7 cassettes per carton, Rx Only, AbbVie Inc., North Chicago, IL 60064 --- NDC 0074-3012-07 — Recall Details · AllClear