China NMPA Product Recall - Skin Graft Carrier

Zimmer Surgical Inc., through its subsidiary Zimmer (Shanghai) Medical International Trading Co., Ltd., has initiated a voluntary Class II recall of its Skin Graft Carriers. This recall, reported on January 11, 2024, addresses discrepancies identified in certain models and batches of the product. The primary issue involves inconsistencies between the actual crease texture and spread ratio of the Skin Graft Carriers and the corresponding information provided on the product labels. The National Medical Products Administration (NMPA) oversees this action, classifying it as a Class II recall, indicating a situation where the use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. Zimmer Surgical Inc. is actively recalling the affected devices to ensure product integrity and patient safety. Customers and healthcare providers are directed to consult 'Medical Device Recall Table 1' and the 'Medical Device Recall Event Report Form' for comprehensive details regarding the specific models, specifications, and batch numbers impacted by this recall. This proactive measure underscores the company's commitment to compliance and quality assurance within the medical device industry.