Aesculap recalls LEFT CORONAL BENDER model TEK1939 used in spinal surgery due to potential deformation of implants. Affected units sold with lot number 2930901A.
Customized coronal rod benders may deform the implant when used with the spinal system devices.
Aesculap recalls a specific spinal surgery tool (LEFT CORONAL BENDER, TEK1939) that may deform spinal implants during use. This could lead to improper spinal alignment if the tool is used incorrectly.
The customized coronal rod benders may deform the spinal implant when used with the spinal system devices. This deformation could lead to improper spinal alignment during surgery, potentially requiring additional procedures.
Surgical teams using the LEFT CORONAL BENDER, TEK1939 during spinal procedures are most at risk. Patients receiving this implant system may be affected if the tool causes improper alignment.
Check for the model number TEK1939 on the LEFT CORONAL BENDER. Affected units were sold with lot number 2930901A.
Identify the model number TEK1939 and lot number 2930901A on the LEFT CORONAL BENDER.
The recall states the tool may deform implants when used with spinal system devices, but does not specify if it's dangerous only under improper use.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected model and lot number.
Check for model number TEK1939 and lot number 2930901A on the LEFT CORONAL BENDER.
We’ve drafted a message you can send Aescul: Aesculap Implant Systems LLC to request your refund or repair — edit it as you like.
Subject: Recall Z-1406-2022 — Aescul: Aesculap Implant Systems LLC Aescul: Aesculap Implant Systems LLC Hello, I own a Aescul: Aesculap Implant Systems LLC that is covered by recall Z-1406-2022 from Aescul: Aesculap Implant Systems LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
