Stryker recalls Hoffmann II Connecting Rod Micro 3 x 90mm (Catalog 50796090) due to potential cracking after cleaning and sterilization. All units are affected.
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Stryker is recalling its Hoffmann II Connecting Rod Micro 3 x 90mm products because they may crack after cleaning and sterilization. This could lead to failure during use, especially in medical procedures.
The connecting rods may crack after cleaning and sterilization, which can happen during routine medical procedures. If the rod cracks during use, it could cause injury to the patient or the surgical team.
Medical professionals who use these connecting rods in surgical procedures are most at risk. Patients using these devices during surgery could be affected if the rods crack.
Check for the catalog number 50796090 on the product. All units produced by Stryker GmbH are affected, including those sold with GTIN 04546540389930.
Look for the catalog number 50796090 or GTIN 04546540389930 on the product.
The Stryker Hoffmann II Connecting Rod Micro 3 x 90mm may crack after cleaning and sterilization, which could lead to failure during use.
Check for the catalog number 50796090 or GTIN 04546540389930 on the product. All units are affected.
The recall does not specify a remedy, so contact Stryker directly for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2831-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2831-2026 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
