Paragon recalls Phantom TTC Nails distributed before sterilization. These medical devices may not be sterile, posing infection risks. Consumers should contact Paragon for details.
Medical devices distributed, prior to sterilization
Paragon is recalling Phantom TTC Nails that were distributed before sterilization. This could lead to infection risks if used without proper sterilization.
Medical devices distributed before sterilization may not be sterile. This could lead to infection risks if used without proper sterilization. The hazard is not described in detail about how it occurs.
Users of Phantom TTC Nails that were distributed before sterilization. Healthcare professionals and medical facilities using these devices are most at risk.
Check for the Phantom TTC Nail model with dimensions 10.0 X 150mm, right side, and reference number P31-600-175L. These were distributed before sterilization.
Reach out to Paragon for specific details about the recalled items and next steps.
The recall is because medical devices were distributed before sterilization, which may not be sterile.
Check for the Phantom TTC Nail model with dimensions 10.0 X 150mm, right side, and reference number P31-600-175L.
Contact Paragon for specific details about the recalled items and next steps.
We’ve drafted a message you can send Paragon to request your refund or repair — edit it as you like.
Subject: Recall Z-1255-2024 — Paragon Paragon Hello, I own a Paragon that is covered by recall Z-1255-2024 from Paragon. 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.
