Merete PediatrOS RigidTack Size 20mm: Incorrect Label on Product
Merete Medical recalls PediatrOS RigidTack size 20mm due to incorrect marketing label (25mm) applied. This affects products sold with the wrong size marking.
Lower-risk recall
Incorrect marketing label (25 mm) was applied to product size 20 mm.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/61255-merete-pediatros-rigidtack-size-20mm-incorrect-label-on-product.
Source Summary by GovInfoNow · govinfonow.com/recall/61255-merete-pediatros-rigidtack-size-20mm-incorrect-label-on-product · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0650-2022
Cite this page
“Merete PediatrOS RigidTack Size 20mm: Incorrect Label on Product.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61255-merete-pediatros-rigidtack-size-20mm-incorrect-label-on-product. Based on FDA recall #Z-0650-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0650-2022%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Merete Medical- Product
Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only- Category
Medical device
What to do — step by step
Check Product Label
Look for the model number CP20120 and lot number MS2117816 on the packaging.
Where it went and when
Where it was distributed
Distributed in Illinois, and outside the U.S.
FDA distribution: “Domestic: Illinois; Foreign: Germany.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0650-2022 (January 18, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0650-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.