Stryker Gmbh: Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
Stryker GmbH is recalling the Hoffmann II Connecting Rod Micro 3 x 40mm (Catalog Number: 50796040), a surgical fixation device used worldwide, because the carbon connecting rods may crack after being cleaned and sterilized. The recall affects devices distributed across the United States and multiple countries including Canada, Australia, and parts of Europe. This is a Class II recall, indicating a moderate health risk.
- Recalling firm
- Stryker GmbH
- Product
- Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.
- Reason
- Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-07-01
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- 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,...
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d5cd761d-a128-47d9-8732-2fe0e95570f7