Leiter's Pharmacy

FDA Regulatory Profile

Leiter's Pharmacy appears in FDA public data with 4 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1041-2013, Class II) was initiated on August 26, 2013.

Summary

Total Recalls
4
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1041-2013Class IILidocaine/Phenylephrine PF 1%/1.5% Injectible vials, 1 mL Single Use Vial, Compounded by Leiter's CoAugust 26, 2013
D-1039-2013Class IIHyaluron (hyaluronidase) 150 units/mL Preserved Solution, 1 mL, Multi Dose Vial, Compounded by LeiteAugust 26, 2013
D-1038-2013Class IIDextrose 50% Preservative Free SDV Injection Solution, 50 mL Single dose vial, IV Administration, CAugust 26, 2013
D-1040-2013Class IIBevacizumab (Avastin) 2.5mg/0.1mL PF Inj., 0.1 mL syringe, Compounded by Leiter's Compounding PharAugust 26, 2013