Merete PediatrOS RigidTack — Class II medical device recall Z-0650-2022
Terminated recall by Merete Medical GmbH, reported 2022-02-23, distributed in IL. Incorrect marketing label (25 mm) was applied to product size 20 mm.
| Recall number | Z-0650-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merete Medical GmbH, Berlin, N/A, Germany |
| Recall initiated | 2022-01-18 |
| Classified | 2022-02-17 |
| Reported by FDA | 2022-02-23 |
| Terminated | 2023-02-16 |
| Distributed | IL |
| Countries outside the US | DE |
| Quantity | 26 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04048266150394 |
| Lot numbers | MS2117816 |
| Model numbers | CP20120 |
Product
Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
Reason for recall
Incorrect marketing label (25 mm) was applied to product size 20 mm.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0650-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.