Stryker Gmbh: Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
Stryker is recalling Hoffmann II Connecting Rod Micro devices (catalog number 50796050) distributed worldwide because the carbon rods may crack during cleaning and sterilization procedures. This Class II recall affects medical facilities across the US and multiple countries including Canada, Australia, and throughout Europe. The devices are orthopedic fixation components used in surgical procedures.
- Recalling firm
- Stryker GmbH
- Product
- Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.
- 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/f50ccea6-bee6-43c8-9f44-b9b54cf45dcd