Methylprednisolone Sodium Succinate · 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9850-01)
Yes — this exact package was recalled
1 FDA recall names the code 0143-9850-01 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
Methylprednisolone Sodium Succinate
Strength
METHYLPREDNISOLONE SODIUM SUCCINATE 500 mg/1
Form
Injection, Powder, for Solution · Intramuscular, Intravenous
Labeling: Incorrect Instructions: Vial label incorrectly instructs healthcare professional to reconstitute product with 16 mL rather than the correct volume of 8 mL of Bacteriostatic Water for Injection with Benzyl Alcohol.
TerminatedLabeling / mix-upHikma Pharmaceuticals USA Inc.NDC 0143-9850-01D-0801-2020
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.
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.