FDA recall D-0806-2016

Meditech Laboratories, Inc · Class II · drug

Product

Formula 3 (Papaverine 20 mg, Phentolamine 3 mg, Atropine 0.2 mg, PGE 20 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.

Reason for recall

Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2016-03-14
Report date
2016-04-13
Termination date
2016-06-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Las Vegas, NV, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0806-2016