TP Orthodontics recalls Jasper Vek: 106 complaints of device breaking in mouth, causing injury risk. Check product model 610-536L for affected units.
The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient.
TP Orthodontics recalls their Jasper Vektor Class II correction appliance (model 610-536L) due to reports of it breaking inside the mouth, which could cause injury. This recall affects patients using the device for correcting class 2 malocclusions.
The device can break inside the mouth, potentially causing injury to the patient. This breakage has been reported in 106 cases, indicating a risk of harm during normal use.
Patients wearing the Jasper Vektor appliance for correcting class 2 malocclusions are most at risk. The recall applies to those who have the specific model number 610-536L.
Check for the model number 610-536L on the appliance. The product is used for correcting class 2 malocclusions by applying light forces on teeth.
Look for the model number 610-536L on the appliance to confirm if it is affected.
TP Orthodontics has received 106 complaints of the device breaking in the patient's mouth, which may cause injury.
Check for the model number 610-536L on the appliance, which is used for correcting class 2 malocclusions.
The recall record does not specify a remedy, so contact TP Orthodontics directly for guidance.
We’ve drafted a message you can send TP Orthodontics to request your refund or repair — edit it as you like.
Subject: Recall Z-1794-2018 — TP Orthodontics TP Orthodontics Hello, I own a TP Orthodontics that is covered by recall Z-1794-2018 from TP Orthodontics. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
