Devices

Device Recall SpheRx Posted Pedicle Screw System

Model / Serial
Batch: JK2036, JK2132, JK2350.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
4.5mm x 40mm Noncannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Manufacturer
NuVasive Inc
1 Event
- Recall of Device Recall SpheRx Posted Pedicle Screw System

Manufacturer

NuVasive Inc

Manufacturer Address
NuVasive Inc, 7475 Lusk Blvd, San Diego CA 92121-5707
Manufacturer Parent Company (2017)
NuVasive, Inc.
Source
USFDA

30 devices with a similar name

Learn more about the data here

Device Recall SpheRx Posted Pedicle Screw System

Model / Serial
Batch: JK2082, JK2095, JK2165
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
5.5mm x 50mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Manufacturer
NuVasive Inc

Device Recall SpheRx Posted Pedicle Screw System

Model / Serial
Batch: JK2059, JK2084, JK2148
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
5.5mm x 55mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Manufacturer
NuVasive Inc

Device Recall SpheRx Posted Pedicle Screw System

Model / Serial
Batch: JK2057, JK2157.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
6.5mm x 30mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Manufacturer
NuVasive Inc

Device Recall SpheRx Posted Pedicle Screw System

Model / Serial
Batch: JK2083, JK2184
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
6.5mm x 35mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Manufacturer
NuVasive Inc

Device Recall SpheRx Posted Pedicle Screw System

Model / Serial
Batch: JK2052, JK2070, JK2098, JK2160, JK2093, JK2159
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
6.5mm x 40mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Manufacturer
NuVasive Inc

25 more

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)