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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Jewel Precision Sterilization Containers Recalled for Incorrect Instructions

Agency Publication Date: June 25, 2025
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Summary

Jewel Precision Sheet Metal & Machining Co, Inc. is recalling 11 units of its Reusable Rigid Sterilization Container System (Model JP-24-6) because the included instructions do not match the FDA-cleared usage guidelines or the product's sterility shelf life. No injuries or incidents have been reported in connection with this issue. These containers were distributed in Indiana, New York, and Pennsylvania.

Risk

Incorrect sterilization instructions or inaccurate shelf-life data can lead to medical instruments not being properly cleaned or remaining sterile, which could cause infections in patients during medical procedures.

What You Should Do

  1. This recall affects the Jewel Precision Reusable Rigid Sterilization Container System, Model/Catalog Number JP-24-6, with GTIN 00850043393016. All lots shipped up to May 23, 2025, are included in this recall.
  2. Stop using the recalled product immediately.
  3. Contact Jewel Precision Sheet Metal & Machining Co, Inc. or your equipment distributor to arrange for a return, replacement, or corrected instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Jewel Precision Reusable Rigid Sterilization Container System
Model / REF:
JP-24-6
GTIN:
00850043393016
Date Ranges: Shipped up to May 23, 2025

Quantity: 11 units. Recall #: Z-2026-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96957
Status: Active
Manufacturer: Jewel Precision Sheet Metal & Machining Co, Inc.
Sold By: specialty retailers
Manufactured In: United States
Units Affected: 11 units
Distributed To: Indiana, New York, Pennsylvania

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.