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
.
ConvaTec Inc.
has voluntarily recalled the foam dressing AQUACEL™ Foam Hydrofiber™ Dressing.
ConvaTec Inc.
has voluntarily recalled the foam dressing AQUACEL™ Foam Hydrofiber™ Dressing (Registration No.
: National Machinery Injection 20173640956)
.
The recall level is three
.
Biomet Orthopedics reported that Zimmer (Shanghai) Medical International Trading Co.
, Ltd.
voluntarily recalled the revision femoral stem and accessories Arcos Modular Revision System and shoulder joint system Comprehensive Shoulder System.
Due to the specific model and specific batch of products, there is a Porous plasma spray coating (PPS) has been wrongly reworked.
20163461304, State Machinery injected 20153463900) voluntarily recalled
.
The recall level is two
.
MAILLEFER INSTRUMENTS HOLDING SARL MAILLEFER INSTRUMENTS HOLDING SARL Dentsply Sirona Dental Products (Shanghai) Co.
, Ltd.
has voluntarily recalled mechanical root canal files and dental files.
Dental Instruments Holding Company 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
.