SET SCREW RETAINING DRIVER, REF 9010000820, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc. Screwdriver - orthopedic manual surgical instrument.
Reported: February 5, 2014 Initiated: January 3, 2014 #Z-0866-2014
Product Description
SET SCREW RETAINING DRIVER, REF 9010000820, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc. Screwdriver - orthopedic manual surgical instrument.
Reason for Recall
The retaining tabs component of the Set Screw Retaining Drive may be oversized, which will not allow proper mating between the Set Screw Retaining Drive and the set screw.
Details
- Recalling Firm
- Medtronic Sofamor Danek USA Inc
- Units Affected
- 7 units
- Distribution
- US Distribution in the states of CA, NC, TX, IN, NJ, and MI.
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
SET SCREW RETAINING DRIVER, REF 9010000820, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc. Screwdriver - orthopedic manual surgical instrument.. Recalled by Medtronic Sofamor Danek USA Inc. Units affected: 7 units.
Why was this product recalled? ▼
The retaining tabs component of the Set Screw Retaining Drive may be oversized, which will not allow proper mating between the Set Screw Retaining Drive and the set screw.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 5, 2014. Severity: Moderate. Recall number: Z-0866-2014.
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