Otto Bock Healthcare Product

FDA Regulatory Profile

Otto Bock Healthcare Product 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-0815-2018, Class II) was initiated on September 12, 2017.

Summary

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

Recent Recalls

NumberClassProductDate
Z-0815-2018Class IIOTTO BOCK Kenevo knee joints Model 3C60=STSeptember 12, 2017
Z-0814-2018Class IIOTTO BOCK Kenevo knee joints Model 3C60September 12, 2017
Z-2438-2015Class IIOtto Bock Healthcare Products GmbH Genium X3 Model Number: 3B5-2, Manufacturer Otto Bock HealthcareAugust 12, 2015