Coltene Whaledent recalls Diatech Diamond dental burs (model 856-016-7-F) due to inconsistent length in a specific batch. Affected units have lot number J22952.
A single batch of Diatech Diamond dental burs, 856-016-7-F, Round end taper, contain diamond burs with the same grit size (fine) and shape (round end taper) but different length.
Coltene Whaledent is recalling a specific batch of Diatech Diamond dental burs (model 856-016-7-F) because they have the same grit size and shape but different lengths. This inconsistency could lead to improper use or damage during dental procedures.
The recalled burs have the same fine grit size and round end taper shape but vary in length within a single batch. This inconsistency could cause improper cutting or damage to dental materials during procedures.
Dental professionals who use the recalled Diatech Diamond burs (model 856-016-7-F) with lot number J22952 are most at risk. Patients using these burs during procedures may also be affected.
Check for the model number 856-016-7-F on the Diatech Diamond burs. The affected batch has lot number J22952. These burs are sold by Coltene /Whaledent AG.
Look for the model number 856-016-7-F and lot number J22952 on the burs.
The recalled batch has the same grit size and shape but different lengths, which could cause improper use during dental procedures.
Check for model number 856-016-7-F and lot number J22952 on the burs.
The recall record does not specify a remedy, so contact Coltene /Whaledent AG for further instructions.
We’ve drafted a message you can send Coltene /Whaledent to request your refund or repair — edit it as you like.
Subject: Recall Z-2436-2019 — Coltene /Whaledent Coltene /Whaledent Hello, I own a Coltene /Whaledent that is covered by recall Z-2436-2019 from Coltene /Whaledent. 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.
