FDA recall record

Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall — FDA Z-2828-2026

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

Class IIclassification
Z-2828-2026official record ID
Aug 5, 2026report date

Recall record at a glance

Official recordZ-2828-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmStryker GmbH
Report dateAug 5, 2026
Recall initiation dateJul 1, 2026
Quantity6,244 units
LocationSelzach, N/A, Switzerland

Official product description

Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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