Jewel Precision Reusable Rigid Sterilization Container System — Class II medical device recall Z-2033-2025
Ongoing recall by Jewel Precision Sheet Metal & Machining Co, Inc., reported 2025-07-02, distributed in TN. The 8-inch model of the Jewel Precision Reusable Rigid Sterilization Container System (i.e., model number: JP-
| Recall number | Z-2033-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Jewel Precision Sheet Metal & Machining Co, Inc., Cedar Grove, NJ, United States |
| Recall initiated | 2025-05-23 |
| Classified | 2025-06-26 |
| Reported by FDA | 2025-07-02 |
| Distributed | TN |
| Quantity | 1 |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00850043393139 |
| Lot numbers | 16899 |
| Model numbers | JP-24-8 |
Product
Jewel Precision Reusable Rigid Sterilization Container System. Model Number: JP-24-8.
Reason for recall
The 8-inch model of the Jewel Precision Reusable Rigid Sterilization Container System (i.e., model number: JP-24-8) was not cleared by the FDA. The letter to file justifying the change in size was insufficient.
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-2033-2025. 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.