Steritec Products Mfc. Co., Inc.

FDA Regulatory Profile

Steritec Products Mfc. Co., Inc. appears in FDA public data with 8 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1827-2013, Class II) was initiated on June 10, 2013.

Summary

Total Recalls
8
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1827-2013Class IIMesa Labs Smart-Read 10^5 EZ Test BI Test Pack, SteriTec Product Code PL 298/25, Distributor ProductJune 10, 2013
Z-1828-2013Class IIMedline Med-Checks BI Test packs with Instant Readout Integrator, SteriTec Product Code PL 200, DistJune 10, 2013
Z-1824-2013Class IIEZTest Steam Biological Indicator, SteriTec Product Code EZS and EZS-400 EZTest Steam Biological June 10, 2013
Z-1829-2013Class IICardinal BI Stat Biological Test Pack with Instant Readout Integrator, SteriTec Product Code PL 160/June 10, 2013
Z-1822-2013Class IIMedline Steam Biological Indicators, SteriTec Product Code PL 353, Distributor Product Code MDS20052June 10, 2013
Z-1823-2013Class IICardinal Steam Biological Indicator, SteriTec Product Code PL 218, Distributor Product Code T40360EZJune 10, 2013
Z-1825-2013Class IIGetinge Assure Accufast BI Test Pack w/ 5 Controls, SteriTec Product Code PL 395, Distributor ProducJune 10, 2013
Z-1826-2013Class IIGetinge Assure Accufast BI Test Pack w/ 25 Controls, SteriTec Product Code PL 395/25, Distributor PrJune 10, 2013