Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.
FDA Recall Z-2831-2026 · Posted 2026-07-29
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Recalling FirmStryker GmbH
Recall StatusOpen, Classified
Product CodeKTT
Date Initiated2026-07-01
Product Quantity9,405 units
Reason for Recall
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Firm Action
Firm began notifying consignees on July 1, 2026.
Customers were instructed to immediately check their internal inventory to locate affected product.
Customers were informed that until further notice, the subject devices are limited to single use only. Following first use, discard the devices in accordance with the facility's established procedures.
Users should conduct visual inspection of product prior to each use.
If cracking is found to be present, the customer should quarantine non-confirming parts and report the issue to Stryker's Trauma & Extremities division. Rods with cracks should be returned as part of the complaint process.
Root Cause
Device Design
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.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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