Hager & Meisinger Gmbh recalls Singles carbides (US No 245) due to possible 1.0mm blade packaged in 0.9mm blade packaging. Affected items have specific model numbers and lot codes.
Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.
Hager & Meisinger Gmbh is recalling Singles carbides (US No 245) because they might have incorrectly packaged a 1.0mm carbide blade in a 0.9mm blade's packaging. This could lead to using the wrong blade size in tools, potentially causing damage or injury.
The recall involves a potential mix-up between 1.0mm and 0.9mm carbide blades. Using the wrong blade size could cause tool damage or improper cutting, but it does not pose a direct risk of injury or serious harm.
Users of Meisinger Singles carbides (US No 245) with specific model numbers and lot codes are affected. People using these carbides in precision cutting tools are most at risk.
Check for the model number US No 245, lot code R23891, and UDI code +E0HM26UN2453140099 on the packaging. This product was sold with specific head size and length specifications.
Look for the model number US No 245, lot code R23891, and UDI code +E0HM26UN2453140099 on the packaging to confirm if it's affected.
The recall is due to a potential mix-up where a 1.0mm carbide blade was packaged in a 0.9mm carbide blade's packaging, which could lead to using the wrong blade size.
Check for the model number US No 245, lot code R23891, and UDI code +E0HM26UN2453140099 on the packaging.
The recall does not specify a remedy, so check the product details to confirm if it's affected and contact the manufacturer if unsure.
We’ve drafted a message you can send Meisinger to request your refund or repair — edit it as you like.
Subject: Recall Z-0493-2020 — Meisinger Meisinger Hello, I own a Meisinger that is covered by recall Z-0493-2020 from 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.
