TP Orthodontics recalls Jasper Vektor Class II Correction Appliance (Part No. 610-530) after 106 complaints of device breaking in patients' mouths, potentially causing injury.
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 (Part No. 610-530) because it has broken in patients' mouths 106 times, which could cause injury. This appliance is used for correcting class 2 malocclusions by applying light forces on teeth.
The appliance can break inside the mouth, which may cause injury to the patient. This has happened 106 times based on complaints from users.
Patients wearing the Jasper Vektor appliance are affected. Those with class 2 malocclusions who use this specific appliance model are most at risk.
Check for the model number 610-530 on the appliance. This product was sold with specific serial numbers: 16015000, 17315000, 17715000, 18115000, 19515000, 24015000, 26515000, 30015000, 32315000, 32815000, 33515000.
Look for the model number 610-530 on the appliance to confirm it is recalled.
TP Orthodontics has received 106 complaints that the device broke in patients' mouths, which could cause injury.
Check for the model number 610-530 on the appliance. This product was sold with specific serial numbers: 16015000, 17315000, 17715000, 18115000, 19515000, 24015000, 26515000, 30015000, 32315000, 32815000, 33515000.
The recall record does not specify a remedy, so no action is required beyond checking if you have the recalled model.
We’ve drafted a message you can send TP Orthodontics to request your refund or repair — edit it as you like.
Subject: Recall Z-1785-2018 — TP Orthodontics TP Orthodontics Hello, I own a TP Orthodontics that is covered by recall Z-1785-2018 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.
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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.
