PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: April 25, 2018 Initiated: March 22, 2018 #D-0645-2018

Product Description

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

Reason for Recall

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

Details

Units Affected
15 vials
Distribution
NV only
Location
Las Vegas, NV

Frequently Asked Questions

What product 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. Recalled by Partell Specialty Pharmacy. Units affected: 15 vials.
Why was this product recalled?
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 25, 2018. Severity: Moderate. Recall number: D-0645-2018.