NMPA Announces Class II Recalls Involving Johnson & Johnson Surgical Vision and Intervascular SAS

China Economic Net, February 21 (Reporter Hanlu) -- On February 21, the National Medical Products Administration (NMPA) released a batch of recall information. The medical device products produced by Johnson & Johnson Surgical Vision and Intel Vensicula Co., Ltd. are involved in a Level II recall.

AMO (SHANGHAI) MEDICAL Devices Trading Co., Ltd. reported that due to issues involving specific models and specific batches of products with non-conforming weld seams, Johnson & Johnson Surgical Vision, Inc. voluntarily recalled the single-use tubing set (ophthalmic phacoemulsification system) (registration certificate number: Guo Med Reg No. 20193160026). The recall level is Class II.

Maquet (Shanghai) Medical Equipment Co., Ltd. reported that due to issues involving specific models and specific batches of products with a slight insufficiency in sterilant dosage, Intervascular SAS has initiated a voluntary recall of the double-velour woven artificial blood vessel (Registration Certificate No.: Guo Med Reg In 20173130601). The recall level is Class II.