FDA Recall Open, Classified

Jewel Precision Reusable Rigid Sterilization Container System. Model Number: JP-24-8.

Recall: Z-2033-2025 · Initiated May 23, 2025

Recall

Recall Number
Z-2033-2025
Event Number
96958
Firm
Jewel Precision Sheet Metal & Machining Co, Inc.
FEI Number
3004112448
Product Code
KCT
Status
Open, Classified
Root Cause
No Marketing Application
Initiated
May 23, 2025
Posted
June 26, 2025
Address
200 Commerce Rd, Cedar Grove, NJ, 07009-1209

Description

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.

Action

Jewel Precision sent a "MEDICAL DEVICE RECALL" letter dated 5/23/2025 to the single consignee on 05/23/2025 via email. The consignee was instructed to; review all stock and inventory, return the product to Jewel Precision for destruction, complete the Acknowledgement and Receipt form on pages 3-4 of the letter indicating the actions taken and approval of completion, in the event that the product has been scrapped, please provide evidence of scrapping it and certification that the product has been destroyed by the customer. As per the customer's purchase order, the piece was to be used for testing purposes only. For products that have been shipped to your customers, identify and notify your customers of the recall, requesting return; obtain their acknowledgement and approval that the part has been shipped back. Action by company: discontinued the product. For questions email: [email protected] or call 973-857-5545 x19.

Distribution

US distribution to Tennessee.

Quantity

1