Electro Medical Systems SA recalls PIEZON Bottle model EG-111 due to risk of disassembly when pressurized during dental treatments or storage. Affected units may leak or cause injury if not properly sealed.
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
Electro Medical Systems SA recalls PIEZON Bottle model EG-111 after complaints that some bottles can disassemble under pressure during dental treatments or storage. This could lead to leaks or injury if the bottle isn't properly sealed.
The bottles can disassemble into two parts when pressurized during dental treatments or storage if the pressure isn't released. This disassembly may cause leaks or injury if the bottle isn't properly sealed.
Dental professionals using PIEZON Bottles for dental treatments are most at risk. Owners of the recalled model EG-111 bottles should check if their units were assembled with a specific batch of bottle collars.
Check for model number EG-111 on the bottle. Affected units were sold with specific batch numbers: Lot 16442-190 (expiry 2026-04) and Lot 16694-30 (expiry 2026-07).
Look for model number EG-111 on the bottle to confirm if it's affected.
Reach out to Electro Medical Systems SA for specific batch numbers and remedy instructions.
The recall is due to complaints that some bottles can disassemble into two parts when pressurized during dental treatments or storage.
Check if your bottle has model number EG-111 and was sold with specific batch numbers (Lot 16442-190 or 16694-30). Contact Electro Medical Systems SA for further instructions.
Yes, if the bottle disassembles during use or storage, it could leak or cause injury if not properly sealed.
We’ve drafted a message you can send PIEZON to request your refund or repair — edit it as you like.
Subject: Recall Z-1688-2024 — PIEZON PIEZON Hello, I own a PIEZON that is covered by recall Z-1688-2024 from PIEZON. 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.
