Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 71288-0712-06 recalled?

Cisatracurium Besylate · 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-712-06) / 5 mL in 1 VIAL, SINGLE-DOSE (71288-712-05)

Yes — this exact package was recalled

1 FDA recall names the code 71288-0712-06 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Cisatracurium Besylate
Strength
CISATRACURIUM BESYLATE 10 mg/5mL
Form
Injection, Solution · Intravenous
Labeler
Meitheal Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
71288-0712

Recalls naming this package

Class I · High risk

Cisatracurium Besylate Injection

Labeling: Label mix-up: Carton of Cisatracurium Besylate Injection, USP was observed to contain ten vials mislabeled as Phenylephrine Hydrochloride Injection, USP, but confirmed to contain Cisatracurium

Terminated Labeling / mix-up Meitheal Pharmaceuticals Inc NDC 71288-712-05 D-0286-2021

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler