Hager & Meisinger recalls SINGLES Carbide US-No. FG556 dental devices due to potential US-dates mismatch between package label and bar code. Affected units have specific identifiers and usage for dental procedures.
US-dates between the product package label and the bar code display.
Hager & Meisinger is recalling SINGLES Carbide US-No. FG556 dental devices because of a potential mismatch between the product's package label dates and bar code dates. This could affect the device's intended use for cutting hard materials in dental procedures.
The hazard involves a potential mismatch between the US-dates on the product package label and the bar code display. This mismatch could lead to incorrect date information affecting the device's intended use for cutting hard materials in dental procedures.
Dental professionals using SINGLES Carbide US-No. FG556 devices for dental procedures are likely affected. Patients using these devices for dental work may be at risk if the dates are mismatched.
Check for the product identifier UDI +E0HM26000313140091, model SINGLES Carbide US-No. FG556, and the lot number R50753. The device is used for cutting hard structures in the mouth, such as teeth or bone.
Verify that the US-dates on the package label match the bar code display to ensure correct date information.
The recall is due to a potential mismatch between the US-dates on the product package label and the bar code display, which could affect the device's intended use for cutting hard materials in dental procedures.
The specific model number is SINGLES Carbide US-No. FG556 with UDI +E0HM26000313140091 and lot number R50753.
The recall record does not specify a remedy.
We’ve drafted a message you can send Hager & Meisinger to request your refund or repair — edit it as you like.
Subject: Recall Z-2937-2020 — Hager & Meisinger Hager & Meisinger Hello, I own a Hager & Meisinger that is covered by recall Z-2937-2020 from Hager & Meisinger. 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.
