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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
.
.
These include foam dressings, valvuloplasty rings, and more
.
Details are as follows:
Edwards Lifesciences LLC Voluntary Recall of Valvuloplasty Ring Tricuspid Annuloplasty Ring
Edwards (Shanghai) Medical Products Co.
, Ltd.
reported that the manufacturer Edwards Lifesciences LLC has made a decision on the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration Certificate No.
: National Instruments) due to the fact that it involves a specific model and a specific batch of products, and the expiration date on the product label is wrong.
Inject 20173466532) voluntary recall
.
The recall level is three
.
, Ltd.
reported that the manufacturer Edwards Lifesciences LLC has made a decision on the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration Certificate No.
: National Instruments) due to the fact that it involves a specific model and a specific batch of products, and the expiration date on the product label is wrong.
Inject 20173466532) voluntary recall
.
The recall level is three
.
ConvaTec Inc Voluntary Recall of AQUACEL ™ Foam Hydrofiber™ Dressing
ConvaTec (China) Medical Products Co.
, Ltd.
reported that due to the problem of a specific model and a specific batch of products, there may be a problem that the product may contain the wrong version of the instruction manual, the manufacturer ConvaTec Inc.
Registration certificate number: National Machinery Injection 20173640956) voluntary recall
.
The recall level is three
.
, Ltd.
reported that due to the problem of a specific model and a specific batch of products, there may be a problem that the product may contain the wrong version of the instruction manual, the manufacturer ConvaTec Inc.
Registration certificate number: National Machinery Injection 20173640956) voluntary recall
.
The recall level is three
.
Biomet Orthopedics voluntarily recalls revision femoral stems and accessories Arcos Modular Revision System , Shoulder System Comprehensive Shoulder System
Zimmer (Shanghai) Medical International Trading Co.
, Ltd.
reported that due to the problem of wrong rework operations on the porous plasma spray coating (PPS) involving specific models and specific batches of products, Biomet Orthopedics Biomet Orthopedics Co.
, Ltd.
Femoral stem and accessories Arcos Modular Revision System, Shoulder Joint System Comprehensive Shoulder System (Registration No.
: National Machinery Injection 20163461304, National Machinery Injection 20153463900) voluntarily recalled
.
The recall level is two
.
, Ltd.
reported that due to the problem of wrong rework operations on the porous plasma spray coating (PPS) involving specific models and specific batches of products, Biomet Orthopedics Biomet Orthopedics Co.
, Ltd.
Femoral stem and accessories Arcos Modular Revision System, Shoulder Joint System Comprehensive Shoulder System (Registration No.
: National Machinery Injection 20163461304, National Machinery Injection 20153463900) voluntarily recalled
.
The recall level is two
.
MAILLEFER INSTRUMENTS HOLDING SARL voluntary recall of mechanical root canal files and dental files
Dentsply Sirona Dental Products (Shanghai) Co.
, Ltd.
reported that due to product packaging sealing problems, the manufacturer MAILLEFER INSTRUMENTS HOLDING SARL Mai Fei Dental Instrument Holdings Co.
, Ltd.
Into 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029) voluntary recall
.
The recall level is three
.
, Ltd.
reported that due to product packaging sealing problems, the manufacturer MAILLEFER INSTRUMENTS HOLDING SARL Mai Fei Dental Instrument Holdings Co.
, Ltd.
Into 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029) voluntary recall
.
The recall level is three
.
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
.
.
These include foam dressings, valvuloplasty rings, and more
.
Details are as follows:
Edwards Lifesciences LLC Voluntary Recall of Valvuloplasty Ring Tricuspid Annuloplasty Ring
Edwards (Shanghai) Medical Products Co.
, Ltd.
reported that the manufacturer Edwards Lifesciences LLC has made a decision on the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration Certificate No.
: National Instruments) due to the fact that it involves a specific model and a specific batch of products, and the expiration date on the product label is wrong.
Inject 20173466532) voluntary recall
.
The recall level is three
.
, Ltd.
reported that the manufacturer Edwards Lifesciences LLC has made a decision on the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration Certificate No.
: National Instruments) due to the fact that it involves a specific model and a specific batch of products, and the expiration date on the product label is wrong.
Inject 20173466532) voluntary recall
.
The recall level is three
.
ConvaTec Inc Voluntary Recall of AQUACEL ™ Foam Hydrofiber™ Dressing
ConvaTec (China) Medical Products Co.
, Ltd.
reported that due to the problem of a specific model and a specific batch of products, there may be a problem that the product may contain the wrong version of the instruction manual, the manufacturer ConvaTec Inc.
Registration certificate number: National Machinery Injection 20173640956) voluntary recall
.
The recall level is three
.
, Ltd.
reported that due to the problem of a specific model and a specific batch of products, there may be a problem that the product may contain the wrong version of the instruction manual, the manufacturer ConvaTec Inc.
Registration certificate number: National Machinery Injection 20173640956) voluntary recall
.
The recall level is three
.
Biomet Orthopedics voluntarily recalls revision femoral stems and accessories Arcos Modular Revision System , Shoulder System Comprehensive Shoulder System
Zimmer (Shanghai) Medical International Trading Co.
, Ltd.
reported that due to the problem of wrong rework operations on the porous plasma spray coating (PPS) involving specific models and specific batches of products, Biomet Orthopedics Biomet Orthopedics Co.
, Ltd.
Femoral stem and accessories Arcos Modular Revision System, Shoulder Joint System Comprehensive Shoulder System (Registration No.
: National Machinery Injection 20163461304, National Machinery Injection 20153463900) voluntarily recalled
.
The recall level is two
.
, Ltd.
reported that due to the problem of wrong rework operations on the porous plasma spray coating (PPS) involving specific models and specific batches of products, Biomet Orthopedics Biomet Orthopedics Co.
, Ltd.
Femoral stem and accessories Arcos Modular Revision System, Shoulder Joint System Comprehensive Shoulder System (Registration No.
: National Machinery Injection 20163461304, National Machinery Injection 20153463900) voluntarily recalled
.
The recall level is two
.
MAILLEFER INSTRUMENTS HOLDING SARL voluntary recall of mechanical root canal files and dental files
Dentsply Sirona Dental Products (Shanghai) Co.
, Ltd.
reported that due to product packaging sealing problems, the manufacturer MAILLEFER INSTRUMENTS HOLDING SARL Mai Fei Dental Instrument Holdings Co.
, Ltd.
Into 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029) voluntary recall
.
The recall level is three
.
, Ltd.
reported that due to product packaging sealing problems, the manufacturer MAILLEFER INSTRUMENTS HOLDING SARL Mai Fei Dental Instrument Holdings Co.
, Ltd.
Into 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029) voluntary recall
.
The recall level is three
.
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
.
.
These include foam dressings, valvuloplasty rings, and more
.
Details are as follows:
Details are as follows: Edwards Lifesciences LLC Voluntary Recall of Valvuloplasty Ring Tricuspid Annuloplasty Ring
Edwards Lifesciences LLC Voluntary Recall of Valvuloplasty Ring Tricuspid Annuloplasty Ring Edwards (Shanghai) Medical Products Co.
, Ltd.
reported that the manufacturer Edwards Lifesciences LLC has made a decision on the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration Certificate No.
: National Instruments) due to the fact that it involves a specific model and a specific batch of products, and the expiration date on the product label is wrong.
Inject 20173466532) voluntary recall
.
The recall level is three
.
, Ltd.
reported that the manufacturer Edwards Lifesciences LLC has made a decision on the valvuloplasty ring Tricuspid Annuloplasty Ring (Registration Certificate No.
: National Instruments) due to the fact that it involves a specific model and a specific batch of products, and the expiration date on the product label is wrong.
Inject 20173466532) voluntary recall
.
The recall level is three
.
ConvaTec Inc Voluntary Recall of AQUACEL ™ Foam Hydrofiber™ Dressing
ConvaTec Inc Voluntary Recall of AQUACEL ™ Foam Hydrofiber™ Dressing ConvaTec (China) Medical Products Co.
, Ltd.
reported that due to the problem of a specific model and a specific batch of products, there may be a problem that the product may contain the wrong version of the instruction manual, the manufacturer ConvaTec Inc.
Registration certificate number: National Machinery Injection 20173640956) voluntary recall
.
The recall level is three
.
, Ltd.
reported that due to the problem of a specific model and a specific batch of products, there may be a problem that the product may contain the wrong version of the instruction manual, the manufacturer ConvaTec Inc.
Registration certificate number: National Machinery Injection 20173640956) voluntary recall
.
The recall level is three
.
Biomet Orthopedics voluntarily recalls revision femoral stems and accessories Arcos Modular Revision System , Shoulder System Comprehensive Shoulder System
Biomet Orthopedics voluntarily recalls revision femoral stems and accessories Arcos Modular Revision System , Shoulder System Comprehensive Shoulder System Zimmer (Shanghai) Medical International Trading Co.
, Ltd.
reported that due to the problem of wrong rework operations on the porous plasma spray coating (PPS) involving specific models and specific batches of products, Biomet Orthopedics Biomet Orthopedics Co.
, Ltd.
Femoral stem and accessories Arcos Modular Revision System, Shoulder Joint System Comprehensive Shoulder System (Registration No.
: National Machinery Injection 20163461304, National Machinery Injection 20153463900) voluntarily recalled
.
The recall level is two
.
, Ltd.
reported that due to the problem of wrong rework operations on the porous plasma spray coating (PPS) involving specific models and specific batches of products, Biomet Orthopedics Biomet Orthopedics Co.
, Ltd.
Femoral stem and accessories Arcos Modular Revision System, Shoulder Joint System Comprehensive Shoulder System (Registration No.
: National Machinery Injection 20163461304, National Machinery Injection 20153463900) voluntarily recalled
.
The recall level is two
.
MAILLEFER INSTRUMENTS HOLDING SARL voluntary recall of mechanical root canal files and dental files
MAILLEFER INSTRUMENTS HOLDING SARL voluntary recall of mechanical root canal files and dental files Dentsply Sirona Dental Products (Shanghai) Co.
, Ltd.
reported that due to product packaging sealing problems, the manufacturer MAILLEFER INSTRUMENTS HOLDING SARL Mai Fei Dental Instrument Holdings Co.
, Ltd.
Into 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029) voluntary recall
.
The recall level is three
.
, Ltd.
reported that due to product packaging sealing problems, the manufacturer MAILLEFER INSTRUMENTS HOLDING SARL Mai Fei Dental Instrument Holdings Co.
, Ltd.
Into 20182550087, National Machinery Injection 20192170561, National Machinery Injection 20172067029) voluntary recall
.
The recall level is three
.
