Published on
May 13, 2022
- 20:42 GMT
Avanos Medical Recalls Cortrak*2 Enteral Access System for Risk of Misplaced Enteral Tubes Could Cause Patient Harm
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Name: Avanos Medical Cortrak*2 Enteral Access System Product Codes and Serial Numbers: See …
Distribution channels:
Healthcare & Pharmaceuticals Industry
