Devices

Device Recall Smith & Nephew

Model / Serial
Lot Numbers: 50388182, 50389253, 50391626, 50392272, 50392407, 50395081, 50395680, 50396197, 50400556, 50401558, 50402228, 50403940, 50406036, 50407582, 50409406, 50413407, 50414970, 50412647, 50415864, 50416801, 50418088, 50420654, 50421030, 50421495
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution - US Nationwide and the countries of: Argentina, AUSTRALIA, AUSTRIA, Belgium, CANADA,CHILE COLOMBIA, Denmark, DUBAI, FINLAND, FRANCE GDC BAAR Distribution,GERMANY, GREECE, INDIA ITALY, KOREA, MALAYSIA, MEXICO, NETHERLAND, NORWAY PORTUGAL, PUERTO RICO, SHANGHAI, SOUTH AFRICA SPAIN, SWEDEN, SWITZERLAND, and UNITED KINGDOM.
Product Description
Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures (COBRAID-blue, COBRAIDblack), sterile || Part Number: 72202896 || Product Usage: intended for use for the || reattachment of soft tissue to bone
Manufacturer
Smith & Nephew, Inc. Endoscopy Division
1 Event
- Recall of Device Recall Smith & Nephew

Manufacturer

Smith & Nephew, Inc. Endoscopy Division

Manufacturer Address
Smith & Nephew, Inc. Endoscopy Division, 150 Minuteman Drive, Andover MA 01810-1031
Source
USFDA

62 devices with a similar name

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Device Recall Smith & Nephew

Model / Serial
Lot Number: 50102446
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
NC, PR
Product Description
Smith & Nephew Drill, 2.7mm for BioRaptor Suture Anchor (non-sterile) || Reference Number: 7210430
Manufacturer
Smith & Nephew, Inc., Endoscopy Div.

Device Recall Smith & Nephew FASTFIX

Model / Serial
Lot Numbers: 50141993, 50145519, 50146091,50146096, 50146362, 50148283, 50146365, 50153066, 50150381
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Foreign: Austria, Germany, France, Italy, Australia
Product Description
FAST-FIX AB Curved Needle Delivery System, Used for meniscal repair. || Product Number: 7209399
Manufacturer
Smith & Nephew, Inc. Endoscopy Division

Device Recall Smith & Nephew

Model / Serial
Product distributed prior to May 5, 2006
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide distribution ---- including states of NM, MO, and TN.
Product Description
Smith & Nephew Hip Positioning System Ref: 72200624 with System Components: || Perineal Post 72200631 || Universal Hip Distractor 72200626 || Knee Holder 72200627 || Well Leg Holder 72200632 || Supine Table Extension 72200629
Manufacturer
Smith & Nephew, Inc. Endoscopy Division

Device Recall Smith & Nephew

Model / Serial
Lot Numbers: All lot numbers lower than 50165371 Expanded Recall: Lot Numbers: 50172224, 50173178, 50173179, 50174332, 50174790, 50175034, 50175829, 50175830
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Austria, China, Germany, Finland, Italy, South Africa, South Korea, Switzerland, UK.
Product Description
4.5 mm TRIVEX System Resector Kit (blade and tubing), 3 per box || Part Number: 7209514
Manufacturer
Smith & Nephew, Inc. Endoscopy Division

Device Recall Smith & Nephew

Model / Serial
Lot Numbers: All lot numbers lower than 50165180 Expanded Recall: Lot Numbers: 50165181, 50168833, 50170484, 50170485, 50173279, 50175080, 50175934, 50175936, 50176896
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Austria, China, Germany, Finland, Italy, South Africa, South Korea, Switzerland, UK.
Product Description
5.5 mm TRIVEX System Resector Kit (blade and tubing), 3 per box || Part Number: 7209515
Manufacturer
Smith & Nephew, Inc. Endoscopy Division

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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