RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Reported: July 27, 2022 Initiated: June 30, 2021 #Z-1405-2022
Product Description
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Reason for Recall
Customized coronal rod benders may deform the implant when used with the spinal system devices.
Details
- Recalling Firm
- Aesculap Implant Systems LLC
- Units Affected
- 2 pieces
- Distribution
- United States: CO
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.. Recalled by Aesculap Implant Systems LLC. Units affected: 2 pieces.
Why was this product recalled? ▼
Customized coronal rod benders may deform the implant when used with the spinal system devices.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 27, 2022. Severity: Moderate. Recall number: Z-1405-2022.
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