AAP Implantate Ag recalls soft tissue retractors with lot numbers I012, I025, I028 due to potential debris retention after use. Affected medical devices may cause tissue damage if not properly removed during surgery.
The company has become aware that the soft tissue retractor is not always removed during the sawing process. This can result in damage to the soft tissue retractor in which abrasion debris can develop and remain in vivo.
AAP Implantate Ag is recalling specific soft tissue retractors that may not be fully removed during surgical procedures. This risk could lead to debris remaining in the body, potentially causing tissue damage.
The soft tissue retractor may not be completely removed during the sawing process. This can cause abrasion debris to develop and stay inside the body, potentially damaging soft tissues.
Medical professionals using the recalled soft tissue retractors during surgery are most at risk. Patients receiving these devices during procedures may be affected if debris remains in the body.
Check for lot numbers I012, I025, or I028 on the product label. The product is a radiolucent soft tissue retractor made by AAP Implantate Ag.
Look for lot numbers I012, I025, or I0:28 on the device label.
The company has become aware that the soft tissue retractor may not be fully removed during the sawing process, which can cause debris to remain in the body.
Debris from the retractor may remain in the body after surgery, potentially causing tissue damage.
Check for lot numbers I012, I025, or I028 on the product label. The product is a radiolucent soft tissue retractor made by AAP Implantate Ag.
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-1675-2020 — AAP Implantate Ag AAP Implantate Ag Hello, I own a AAP Implantate Ag that is covered by recall Z-1675-2020 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.
