Recalls / Class II
Class IID-0645-2018
Product
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
- Affected lot / code info
- Lot#: 20180212@22, BUD 03/29/2018; 20180226@64, BUD 04/02/2018.
Why it was recalled
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recalling firm
- Firm
- Partell Specialty Pharmacy
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 5835 S Eastern Ave Ste 101, Las Vegas, Nevada 89119-3031
Distribution
- Quantity
- 15 vials
- Distribution pattern
- NV only
Timeline
- Recall initiated
- 2018-03-22
- FDA classified
- 2018-04-17
- Posted by FDA
- 2018-04-25
- Terminated
- 2019-01-15
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0645-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.