AAP Implantate Ag recalls INTEGRA Drill CS 4.0 (REF 430425) due to incorrect instructions for use. Consumers should check product details and contact the company for guidance.
Products were distributed with the incorrect instructions for use.
AAP Implantate Ag is recalling INTEGRA Drill CS 4.0 (REF 430425) because the product came with the wrong instructions for use. This could lead to improper use if the instructions are not followed correctly.
The product was distributed with incorrect instructions for use, which could lead to improper operation. This might cause the device to function incorrectly during medical procedures, potentially affecting safety and effectiveness.
Users of the INTEGRA Drill CS 4.0 (REF 430425) with incorrect instructions are affected. Medical professionals or individuals using this device for procedures may be at risk if they follow the wrong instructions.
Check for the product name 'INTEGRA Drill CS 4.0', reference number REF 430425, and lot code QS0007. The recall applies to devices sold with the incorrect instructions.
Identify the product name, reference number, and lot code to confirm if your device is affected.
The product was distributed with incorrect instructions for use, which could lead to improper operation during medical procedures.
Check the product details to see if it matches the recall criteria. Contact AAP Implantate Ag for further guidance.
The recall does not specify a fix; the remedy is null, so users should check the product details and contact the manufacturer.
We’ve drafted a message you can send AAP Implantate Ag to request your refund or repair — edit it as you like.
Subject: Recall Z-0732-2020 — AAP Implantate Ag AAP Implantate Ag Hello, I own a AAP Implantate Ag that is covered by recall Z-0732-2020 from AAP Implantate Ag. 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.
