Jewel Precision JP-24-6 sterilization containers recalled due to FDA clearance mismatch. Risk of incorrect use affecting sterility. Stop using if purchased before May 23, 2025.
The Instructions for Use do not match the 510(k) FDA cleared indications for use or sterility shelf life.
Jewel Precision's reusable sterilization containers (model JP-24-6) are recalled because their instructions don't match FDA-approved uses or sterility duration. This could lead to improper sterilization if used without following the correct guidelines.
The product's instructions don't align with the FDA's approved medical uses or how long the containers stay sterile. This mismatch could cause improper sterilization if users follow the wrong instructions.
Healthcare facilities and medical professionals who use these containers for sterilization. Those who purchased containers with model number JP-24-6 shipped before May 23, 2025, are most at risk.
Check for model number JP-24-6 on the container. Containers shipped before May 23, 2025, are affected. The GTIN code 00850043393016 is also associated with this recall.
Look for model number JP-24-6 on the container or packaging.
Confirm the container was shipped before May 23, 2025, as this is the cutoff date for affected units.
The instructions for use don't match the FDA's approved medical uses or sterility shelf life, which could lead to improper sterilization.
Check for model number JP-24-6 and ensure it was shipped before May 23, 2025. The GTIN 00850043393016 is also associated with this recall.
The recall record doesn't specify a remedy, so contact Jewel Precision directly for guidance.
We’ve drafted a message you can send Jewel Precision to request your refund or repair — edit it as you like.
Subject: Recall Z-2026-2025 — Jewel Precision Jewel Precision Hello, I own a Jewel Precision that is covered by recall Z-2026-2025 from Jewel Precision. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
