Recall archive / FDA device enforcement
Jewel Precision Reusable Rigid Sterilization Container System. Model Number: JP-24-8. — FDA record Z-2033-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date May 23, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Jewel Precision Reusable Rigid Sterilization Container System. Model Number: JP-24-8.
- Reason
- 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.
- Classification
- Class II
- Recalling firm
- Jewel Precision Sheet Metal & Machining Co, Inc.
- Quantity
- 1
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2033-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Model No JP-24-8. GTIN: 00850043393139. Lot Number: 16899 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US distribution to Tennessee.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jul 2, 2025
- Recall initiation date
- May 23, 2025
- Center classification date
- Jun 26, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.