FDAJuly 14, 2023drug

succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.

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

The hazard

Lack of assurance of sterility. Validation data for decontamination cycles is lacking.

What to do

FDA enforcement status: Terminated

Brands named

central admixture pharmacy servicescentralcentral admixture

Recall history

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

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