Right Coronal Bender recall
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Why was Right Coronal Bender recalled?
Customized coronal rod benders may deform the implant when used with the spinal system devices.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
LOT: 2930902A
- Product
- RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
- Recalling firm
- Aesculap Implant Systems LLC
- Quantity
- 2 pieces
- Distribution
- United States: CO
- Recall date
- July 27, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)