Reported Jul 27, 2022 · Terminated
LEFT CORONAL BENDER, TEK1939. Instrument used during spinal surgery.
Aesculap Implant Systems LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aesculap Implant Systems LLC · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
- LEFT CORONAL BENDER, TEK1939. Instrument used during spinal surgery.
- Lot codes and dates
- LOT2930901A
- Amount recalled
- 2 pieces
This recall covers 14 products
The agency filed one notice per product. You are reading one of them; the other 13 are below.
1 more are in the archive.
Where it was sold
Why it was recalled
Customized coronal rod benders may deform the implant when used with the spinal system devices.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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