Merete Medical recalls PediatrOS RigidTack size 20mm due to incorrect marketing label (25mm) applied. This affects products sold with the wrong size marking.
Incorrect marketing label (25 mm) was applied to product size 20 mm.
Merete Medical is recalling PediatrOS RigidTack size 20mm products because they were labeled as 25mm. This labeling error could cause confusion about the correct size for medical use.
The product was labeled as 25mm when it is actually 20mm. This incorrect labeling could lead to using the wrong size device during medical procedures, potentially causing complications.
Healthcare providers who use this product for medical procedures may be affected. Patients using the product under a prescription are at risk of incorrect size application.
Check for the model number CP20120 and lot number MS2117816 on the product packaging. Products sold with the label '25mm' instead of '20mm' are affected.
Look for the model number CP20120 and lot number MS2117816 on the packaging.
The product is safe to use but has an incorrect label that may cause confusion about the correct size.
Check the product label for model number CP20120 and lot number MS2117816. If labeled as 25mm, contact Merete Medical for guidance.
Products with model number CP20120 and lot number MS2117816 that are labeled as 25mm instead of 20mm are affected.
We’ve drafted a message you can send Merete Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0650-2022 — Merete Medical Merete Medical Hello, I own a Merete Medical that is covered by recall Z-0650-2022 from Merete Medical. 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.
