Dental EZ Group recalls Titan Scaler Tip model 261: Oversized tip holder may cause injury during use. Affected units sold with specific lot numbers and date codes.
Tip holder portion of the scaler tip assembly may have an oversized condition that will not allow the scaler tip to stay seated in the holder may cause injury
Dental EZ Group is recalling Titan Scaler Tip model 261669 due to a potential oversized tip holder that could cause injury. This affects dental professionals using the scaler tip for subgingival scaling.
The tip holder portion of the scaler tip assembly may be oversized, causing the scaler tip to become dislodged from the holder. This dislodgement could lead to injury during dental procedures.
Dental professionals who use the Titan Scaler Tip model 261669 for subgingival scaling are most at risk. The recall affects specific units sold with lot number 4881439 and date code stamp P424.
Check for the model number 261669 on the scaler tip. Affected units were sold with lot number 4881439 and date code stamp P424.
Inspect the tip holder to ensure the scaler tip stays seated properly. If it becomes loose, stop using the tip immediately.
The recall states the tip holder may be oversized, causing the scaler tip to become dislodged and potentially causing injury. However, the hazard does not specify a risk of serious injury in normal use.
Check for model number 261669 on the scaler tip. Affected units were sold with lot number 4881439 and date code stamp P424.
The recall does not specify a remedy, so you should check the tip holder for dislodgement risk and stop using it if loose.
We’ve drafted a message you can send Dental EZ Group to request your refund or repair — edit it as you like.
Subject: Recall Z-2177-2024 — Dental EZ Group Dental EZ Group Hello, I own a Dental EZ Group that is covered by recall Z-2177-2024 from Dental EZ Group. 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.
