State Food and Drug Administration: Medical devices such as Kangwei De, Bonmei Orthopedics, Edwards are being recalled

On January 20, the State Food and Drug Administration issued an announcement informing that four companies including Convid and Edward have voluntarily recalled some of their illegal products
.
These include foam dressings, valvuloplasty rings, and more
.
The details are as follows: Edwards Lifesciences LLC voluntarily recalled the valvuloplasty ring Tricuspid Annuloplasty Ring Edwards (Shanghai) Medical Supplies Co.
, Ltd.
reported that due to a specific model and a specific batch of products, there was an error in the expiration date on the product label, the manufacturer Edwards Lifesciences LLC voluntarily recalled the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration No.
: National Machinery Injection 20173466532)
.
The recall level is three
.
Attachment: Medical Device Recall Incident Report Form ConvaTec Inc's voluntary recall of AQUACEL™ Foam Hydrofiber™ Dressing to ConvaTec Inc.
ConvaTec Inc's report on the active recall of ConvaTec (China) Medical Products Co.
, Ltd.
Due to the problem of the wrong version of the instructions, the manufacturer, ConvaTec Inc, voluntarily recalled the foam dressing AQUACEL™ Foam Hydrofiber™ Dressing (Registration No.
: National Machinery Injection 20173640956)
.
The recall level is three
.
Attachment: Medical Device Recall Incident Report Form Biomet Orthopedics Biomet Orthopedics Co.
, Ltd.
voluntarily recalled the revision femoral stem and accessories Arcos Modular Revision System, shoulder joint system Comprehensive Shoulder System report by Zimmer (Shanghai) Medical International Trade Co.
, Ltd.
, Certain batches of products, there is an issue of wrong rework operations on the porous plasma spray coating (PPS).
Registration certificate number: National Machinery Injection 20163461304, National Machinery Injection 20153463900) voluntary recall
.
The recall level is two
.
Attachment: Medical Device Recall Incident Report Form The manufacturer, MAILLEFER INSTRUMENTS HOLDING SARL, has voluntarily recalled mechanical root canal files and dental files (registration certificate number: National Machinery Injection 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029)
.
The recall level is three
.
Attachment: Medical Device Recall Incident Reporting Form