CLASS II ONGOING Device recall · Reported 15 Nov 2023 · FDA Enforcement Report
Contra Gray (soft) Turbo Plus Cups recalled
Young Dental Manufacturing I is recalling Contra Gray (soft) Turbo Plus Cups, distributed in Indiana, Missouri, Tennessee. The recall was initiated on 6 Oct 2023 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-0285-2024
- FDA event ID
- 93176
- Recalling firm
- Young Dental Manufacturing I, Earth City, MO
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 6 Oct 2023
- FDA classified
- 9 Nov 2023
- Reported
- 15 Nov 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Dental Devices
Timeline
| 6 Oct 2023 | Recall initiated by company | |
| 9 Nov 2023 | Classified by FDA | +34 days |
| 15 Nov 2023 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
one lot of Contra Gray (soft) Turbo Plus Cups Dental Prophylaxis Angles may contain Contra Petite Web LF Soft Purple Cup DPAs.
Product as listed by the FDA
CONTRA GRAY (soft) TURBO PLUS CUPS, REF 153112. Dental Prophylaxis Angles
Where it was distributed
US: IN, TN, MO
Questions about this recall
Why was it recalled?
one lot of Contra Gray (soft) Turbo Plus Cups Dental Prophylaxis Angles may contain Contra Petite Web LF Soft Purple Cup DPAs.
Which lots are affected?
UDI/DI 10302731631127, Lot Number 223466
Where was it sold?
US: IN, TN, MO
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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