FDA Drug Recalls

Recalls / Firms / Meditech Laboratories, Inc

Meditech Laboratories, Inc

7 FDA drug recalls on record.

DateClassDrugStatus
2016-03-14Class IIFormula 0 (PGE 20 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 320Terminated
2016-03-14Class IIFormula 4 (Papaverine 18 mg, Phentolamine 2 mg, Atropine 0.2 mg/mL) Injection, 5 mL vials,Terminated
2016-03-14Class IIFormula 2 (Papaverine 9 mg, Phentolamine 1 mg, Atropine 0.1 mg, PGE 10 mcg/mL), 5 mL vialsTerminated
2016-03-14Class IIFormula 1 (Papaverine 1.8 mg, Phentolamine 0.2 mg, Atropine 0.02 mg, PGE 18 mcg/mL) InjectTerminated
2016-03-14Class IIFormula 9 (Papaverine 0.9 mg, Phentolamine 0.1 mg, Atropine 0.01 mg, PGE 20 mcg/mL) InjectTerminated
2016-03-14Class IIFormula 2 (Papaverine 9 mg, Phentolamine 1 mg, Atropine 0.1 mg, PGE 10 mcg/mL) Injection, Terminated
2016-03-14Class IIFormula 3 (Papaverine 20 mg, Phentolamine 3 mg, Atropine 0.2 mg, PGE 20 mcg/mL) Injection,Terminated
Meditech Laboratories, Inc — FDA drug recalls (7) · FDA Drug Recalls