Partell Specialty Pharmacy recalls TM #1 (ALP 5.9/PAPAV 17.65/PHEN 0.59) Injectable solution, packaged in 3 mL amber vial, Rx only, Partell Specialty Phar…

Recall date

March 22, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0645-2018

FDA classification

Class II

Brand / firm

Partell Specialty Pharmacy

Sold / distributed

NV only

Why it was recalled

Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

TM #1 (ALP 5.9/PAPAV 17.65/PHEN 0.59) Injectable solution, packaged in 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800