PlainRecalls
FDA Devices Moderate Class II Terminated

iTotal Hip Replacement System, Model HBS-033-0015-020101, Size 15 Hip-Patient Specific Stem Right

Reported: October 16, 2019 Initiated: August 22, 2019 #Z-0063-2020

Product Description

iTotal Hip Replacement System, Model HBS-033-0015-020101, Size 15 Hip-Patient Specific Stem Right

Reason for Recall

Two femoral stems, sizes 13 and 15, were erroneously switched and packed in each other's packaging.

Details

Recalling Firm
Conformis, Inc.
Units Affected
1
Distribution
Distributed to consignees in MD and NV.
Location
Billerica, MA

Frequently Asked Questions

What product was recalled?
iTotal Hip Replacement System, Model HBS-033-0015-020101, Size 15 Hip-Patient Specific Stem Right. Recalled by Conformis, Inc.. Units affected: 1.
Why was this product recalled?
Two femoral stems, sizes 13 and 15, were erroneously switched and packed in each other's packaging.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 16, 2019. Severity: Moderate. Recall number: Z-0063-2020.