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FDAApril 13, 2022drug

Propofol Injectable Emulsion, USP, 200 mg/ 20 mL (10 mg/mL), packaged in a) 50 mL vial, in packs of 20 (NDC 00591-2136-51), b) 100 mL vial, in packs of 10 (NDC 00591-2136-68), Rx only, MFG: Teva Pharma USA

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

The hazard

cGMP deviations: Temperature abuse

What to do

FDA enforcement status: Terminated

Brands named

mckesson medical surgical inc corporate officemckessonmckesson medical

UPCs

0059121365100591213668

Recall history

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

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