Z-2831-2026 Class II Ongoing

Recalled by Stryker GmbH — Selzach, N/A

FDA device recall Z-2831-2026 was initiated by Stryker GmbH on July 1, 2026 and is designated Class II. Reason for recall: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. The recall status is ongoing. Affected quantity: 9,405 units.

Recall Details

Product Type
Devices
Report Date
August 5, 2026
Initiation Date
July 1, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
9,405 units

Product Description

Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.

Reason for Recall

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Distribution Pattern

Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, ID, IL, KS, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NY, OH, PA, RI, SC, TN, TX, VA, WI, WV and the countries of Australia, Austria, Belgium, Canada, Chile, Denmark, France, Germany, Greece, Ireland, Israel, Italy, Japan, Kuwait, Netherlands, Poland, Portugal, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, UK.

Code Information

Catalog Number: 50796090. GTIN: 04546540389930. All lot numbers.