PlainRecalls
FDA Devices Moderate Class II Completed

Exactech BIOLOX delta Femoral Head, 36m O.D. + 3.5mm, REF 170-36-03. Hip prosthesis component.

Reported: August 18, 2021 Initiated: June 29, 2021 #Z-2251-2021

Product Description

Exactech BIOLOX delta Femoral Head, 36m O.D. + 3.5mm, REF 170-36-03. Hip prosthesis component.

Reason for Recall

Biolox Delta Femoral Head was packaged and labeled as 170-36-00 (36mm +0), but the device was marked as 170-36-03 (36mm +3.5).

Details

Recalling Firm
Exactech, Inc.
Units Affected
30 devices
Distribution
US Nationwide Distribution
Location
Gainesville, FL

Frequently Asked Questions

What product was recalled?
Exactech BIOLOX delta Femoral Head, 36m O.D. + 3.5mm, REF 170-36-03. Hip prosthesis component.. Recalled by Exactech, Inc.. Units affected: 30 devices.
Why was this product recalled?
Biolox Delta Femoral Head was packaged and labeled as 170-36-00 (36mm +0), but the device was marked as 170-36-03 (36mm +3.5).
Which agency issued this recall?
This recall was issued by the FDA Devices on August 18, 2021. Severity: Moderate. Recall number: Z-2251-2021.