G & H Wire Company recalls FLEXSelect 5/1:16" Amber Latex Elastics due to mislabeling as non-latex, risking allergic reactions in latex-sensitive patients.
Latex elastic bands were labeled as non-latex elastic bands, an allergic rx can occur due to patient latex allergy
G & H Wire Company is recalling FLEXSelect 5/16" Amber Latex Elastics because they were labeled as non-latex but contain latex, which can cause allergic reactions in sensitive individuals. This affects orthodontic patients using these elastics for braces or tooth gaps.
The elastics are mislabeled as non-latex but contain actual latex. For patients with latex allergies, this can trigger allergic reactions such as skin irritation or more severe symptoms.
Orthodontic patients using braces or tooth gap treatments with the recalled elastics are most at risk. The recall applies to those who purchased the product with the reference number AMD56.
Check for the product name 'FLEXSelect 5/16" Amber Latex Elastics' with reference number AMD56. The lot number is 1120035, and the product was sold with the unique identifier 10195291042642.
Verify the product name, reference number AMD56, and lot number 1120035 to confirm if you have the recalled item.
The elastics were mislabeled as non-latex but contain latex, which can cause allergic reactions in patients with latex allergies.
Orthodontic patients with latex allergies who use the elastics for braces or tooth gaps.
Look for the product name 'FLEXSelect 5/16" Amber Latex Elastics' with reference number AMD56 and lot number 1120035.
We’ve drafted a message you can send G & H Wire Company to request your refund or repair — edit it as you like.
Subject: Recall Z-0976-2024 — G & H Wire Company G & H Wire Company Hello, I own a G & H Wire Company that is covered by recall Z-0976-2024 from G & H Wire Company. 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.
