Fresh Recalls

FDAClass II · Medical device · Recall Z-2829-2026 · Recalled August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall — Stryker GmbH

Agency report date: August 5, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Stryker Hoffmann II Connecting Rod Micro 3 x 50mm
Company / brand
Stryker
Lot / serial / date codes
Catalog Number: 50796050. GTIN: 04546540389916. All lot numbers.
Distribution
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.
Agency product description and boundaries

Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Stryker Hoffmann II Connecting Rod Micro 3 x 50mm

3. Open the official notice or contact

Official recall ID
Z-2829-2026
Brand
Stryker
Classification
Class II
Units affected
7,571 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Selzach, N/A, Switzerland
Firm address
Bohnackerweg 1, N/A, N/A

Identifying details (verbatim from the notice)

Product codes / lots
Catalog Number: 50796050. GTIN: 04546540389916. All lot numbers.
Distribution
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.
Firm notified the public via
Letter
FDA event ID
99246
Recall initiated
July 1, 2026
FDA classified
July 29, 2026
FDA report date
August 5, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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