Mizuho OSI: Medical Device Recall in 2022 - (Recall #: Z-1573-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144

Product Classification:

Class II

Date Initiated: July 29, 2021

Date Posted: August 31, 2022

Recall Number: Z-1573-2022

Event ID: 90603

Reason for Recall:

One batch of "regular" femoral hooks were incorrectly etched with the "classic" femoral hook model number.

Status: Ongoing

Product Quantity: 13 devices

Code Information:

Model Number: 6850-144 UDI Code: (01)00842430106842(10)MIZ210712(11)210712 Lot/Batch Number: MIZ210712

Distribution Pattern:

U.S Nationwide Distribution .: CA, FL, GA, MI, NE, NJ, TN, UT, and WA O.U.S.: Canada

Voluntary or Mandated:

Voluntary: Firm initiated