Devices

Device Recall CERCLAGE WIRE

Model / Serial
Lot Number: 10DM13784
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
KY, TX, DC, NC, CA, AZ, GA and OH; 3 International: Australia, Malaysia, and Switzerland
Product Description
CERCLAGE WIRE, 0.6 MM DIA. X 175 MM LENGTH, SST, REF 71163006, QTY: (6), STERILE R, CE 008, 2020/07, Smith & Nephew, Inc., Memphis, TN 38116, EC REP: Smith & Nephew Orthopaedics GmbH, Tuttlingen, Germany || Usage: Bone fracture fixation
Manufacturer
Smith & Nephew Inc
1 Event
- Recall of Device Recall CERCLAGE WIRE

Manufacturer

Smith & Nephew Inc

Manufacturer Address
Smith & Nephew Inc, 1450 E. Brooks Rd, Memphis TN 38116
Manufacturer Parent Company (2017)
Smith & Nephew plc
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall CERCLAGE WIRE

Model / Serial
Lot Number: 10DM08157
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
KY, TX, DC, NC, CA, AZ, GA and OH; 3 International: Australia, Malaysia, and Switzerland
Product Description
CERCLAGE WIRE, 0.8 MM DIA. X 200 MM LENGTH, SST, REF 71163008, QTY: (6), STERILE R, CE 008, 2020/07, Smith & Nephew, Inc., Memphis, TN 38116, EC REP: Smith & Nephew Orthopaedics GmbH, Tuttlingen, Germany || Usage: Bone fracture fixation
Manufacturer
Smith & Nephew Inc

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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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