Baxa Corporation

FDA Regulatory Profile

Baxa Corporation appears in FDA public data with 3 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2165-2013, Class II) was initiated on August 22, 2013.

Summary

Total Recalls
3
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2165-2013Class IIBaxa Vial Adapter, 14mm - Luer Lock, Order No. REF: 90, Quantity: 50 each, Single Use. Product Code August 22, 2013
Z-1752-2013Class IIExactaMix 1200 and 2400 Compounders. Used as an automated pumping system that compounds multiple June 4, 2013
Z-0156-2013Class IIRepeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstOctober 3, 2012