FDA Class II · Medical device · July 29, 2026
Brand Name recall — Prismatik Dentalcraft, Inc.
Due to device not having FDA Clearance
Official ID Z-2769-2026 · Official record ↗
Prismatik Dentalcraft recalls
Recall found. Prismatik Dentalcraft is named in FDA Class II recall Z-2769-2026 covering Brand Name. Hazard: Due to device not having FDA Clearance Identifying details: Item Number: NITESL UDI-DI code: D745SILNT0 Lot/Serial Numbers: 1020214577 1020784354 1030007997 1030439672 1030523763 1030722759 1106770735 1107310424 1107642834 1108530251 1110784932 1117400787 1118814629 1121913952 1122251905 1122958036 1124408531 1125495087 1127571733 1131149684. Status: Ongoing.
Models with recalls
All Prismatik Dentalcraft recalls
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.