DYNJP2419
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
DYNJP2419
This product is not dangerous
All
Check for the following: UDI-DI: 10080196900107(each), 40080196900108(case), Lot Number: 30525070148
Ensure the UDI-DI matches the product specifications and the Lot Number is within the valid range.
The UDI-DI for DYNJP2419 is 10080196900107(each), 40080196900108(case).
The Lot Number for DYNJP2419 is 30525070148.
We’ve drafted a message you can send DYNJP2419 to request your refund or repair — edit it as you like.
Subject: Recall Z-1423-2026 — DYNJP2419 DYNJP2419 Hello, I own a DYNJP2419 that is covered by recall Z-1423-2026 from DYNJP2419. 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.
