PREAT NOBIL GRIP — Class III medical device recall Z-1226-2023
Ongoing recall by Preat Corp, reported 2023-03-15, distributed nationwide. Product is labeled with an incorrect expiration date.
| Recall number | Z-1226-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Preat Corp, Santa Maria, CA, United States |
| Recall initiated | 2023-02-01 |
| Classified | 2023-03-06 |
| Reported by FDA | 2023-03-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 652 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00842092127308, 00842092155660 |
| Lot numbers | 194397, 21V0089 |
Product
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.
Reason for recall
Product is labeled with an incorrect expiration date.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1226-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.