CLASS II ONGOING Device recall · Reported 3 Jul 2024 · FDA Enforcement Report
Titan Scaler Tip - Perio recalled by Dental EZ Group Star Dental
Dental EZ Group Star Dental Division is recalling Titan Scaler Tip - Perio, distributed nationwide in the US. The recall was initiated on 30 May 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2177-2024
- FDA event ID
- 94783
- Recalling firm
- Dental EZ Group Star Dental Division, Lancaster, PA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 30 May 2024
- FDA classified
- 24 Jun 2024
- Reported
- 3 Jul 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 30 May 2024 | Recall initiated by company | |
| 24 Jun 2024 | Classified by FDA | +25 days |
| 3 Jul 2024 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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
Product as listed by the FDA
Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of mandibular incisors and deep local pockets.
Where it was distributed
US Nationwide distribution.
Questions about this recall
Why was it recalled?
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
Which lots are affected?
UDI-DI D702261669 Lot Number 4881439 Date code stamp P424
Where was it sold?
US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 94783| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Perio recalled | Dental EZ Group Star Dental Division | Packaging Defects | Nationwide |
More recalls from Dental EZ Group Star Dental Division
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Perio recalled | Dental EZ Group Star Dental Division | Packaging Defects | Nationwide |
| Device | CLASS II | Titan T 5K Motor recalled by Dental EZ Group Star Dental | Dental EZ Group Star Dental Division | Other | 7 states |
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