Ormco recalls Damon Q2 orthodontic brackets with mislabeled torque specifications. Affected units may have incorrect torque settings that could impact treatment safety.
The bracket torque was mislabeled on the packaging.
Ormco is recalling specific Damon Q2 orthodontic metal brackets due to mislabeled torque specifications on the packaging. This could lead to improper tooth movement during orthodontic treatment if the brackets are used without the correct torque settings.
The brackets have mislabeled torque specifications on the packaging, which could result in incorrect tooth movement during orthodontic treatment. This might cause discomfort or treatment complications if the brackets are not properly adjusted to the required torque levels.
Orthodontic patients who have received the specific Damon Q2 brackets with part number 491-9834 and lot number 031902599 are affected. Patients using these brackets for orthodontic treatment are at risk if the torque settings are incorrect.
Check for the part number 491-9834 and lot number 031902599 on the bracket packaging. The brackets were manufactured by Ormco Corporation and are intended for temporary use in orthodontic treatment.
Look for the part number 491-9834 and lot number 031902599 on the bracket packaging.
The brackets have mislabeled torque specifications on the packaging, which could lead to incorrect tooth movement during orthodontic treatment.
Check for the part number 491-9834 and lot number 031902599 on the bracket packaging.
The recall does not specify a remedy, so you should contact Ormco directly for guidance.
We’ve drafted a message you can send Ormco to request your refund or repair — edit it as you like.
Subject: Recall Z-2286-2020 — Ormco Ormco Hello, I own a Ormco that is covered by recall Z-2286-2020 from Ormco. 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.
