Stryker Hoffmann II Connecting Rod Recall
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Stryker GmbH is recalling 9,658 units of the Hoffmann II Connecting Rod Micro 3 x 60mm due to potential cracking after cleaning and sterilization.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 13, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Stryker GmbH initiated a voluntary recall of the Stryker Hoffmann II Connecting Rod Micro 3 x 60mm due to potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. The recall is classified as Class II.
Which Products Are Affected
The affected product is Stryker Hoffmann II Connecting Rod Micro 3 x 60mm, Catalog Number: 50796060, GTIN: 04546540389923. All lot numbers are included. A total of 9,658 units are affected. Distribution includes US nationwide 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.
What You Should Do
Contact Stryker GmbH regarding the recall.
Why This Matters
The recall involves 9,658 units distributed worldwide, including extensive US nationwide coverage.
Source
FDA recall number Z-2830-2026. https://www.fda.gov
Original source: FDA Official Notice ↗
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