Aesculap Hasson trocar recalled due to sterility packaging concerns
Aesculap Inc has recalled Hasson trocar surgical instruments (18 units) because sterile blister packaging may be damaged and sterility compromised. The recall affects the U.S. (Kansas, New Jersey, New York) and Canada.
- Product
- DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
- Category
- Medical Device
- Distribution
- Distributed nationwide