Meta C.G.M. Spa recalls specific SAFESCRAPER CURVE TWIST devices used in oral surgery due to potential sterility issues. Devices may not have been adequately sterilized, risking infection.
Sterility issues; single use devices labeled as sterile may not have been adequately sterilized
Meta C.G.M. Spa is recalling certain SAFESCRAPER CURVE TWIST devices used in oral surgery because they may not have been properly sterilized. This could lead to infection risks for patients during procedures.
The devices are labeled as sterile but may not have been adequately sterilized during manufacturing. This could result in infection if used in oral surgery procedures without proper sterilization.
Patients and dental professionals who use the recalled SAFESCRAPER CURVE TWIST devices in oral surgery procedures. Those using the specific lot numbers listed are most at risk.
Check for the model name 'SAFESCRAPER CURVE TWIST' and the lot numbers listed: 10-10719, 25-31118, 23-27018, 16-17118, 15-17018, 2-01521, 23-26620, 23-26820, 17-17920, 7-06519, 17-19818, and 13-12818.
Look for the lot numbers listed in the recall: 10-10719, 25-31118, 23-27018, 16-17118, 15-17018, 2-01521, 23-26620, 23-26820, 17-17920, 7-06519, 17-19818, and 13-12818.
The devices may not have been adequately sterilized, which could lead to infection risks during oral surgery procedures.
The recall does not specify a remedy, so check the lot number and contact the manufacturer if you have the listed lot numbers.
Yes, if the device is not properly sterilized, it could cause infection during oral surgery procedures.
We’ve drafted a message you can send Meta C.G.M. Spa to request your refund or repair — edit it as you like.
Subject: Recall Z-1776-2021 — Meta C.G.M. Spa Meta C.G.M. Spa Hello, I own a Meta C.G.M. Spa that is covered by recall Z-1776-2021 from Meta C.G.M. Spa. 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.
