Recall archive / FDA device enforcement
Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only — FDA record Z-0650-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jan 18, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
- Reason
- Incorrect marketing label (25 mm) was applied to product size 20 mm.
- Classification
- Class II
- Recalling firm
- Merete Medical GmbH
- Quantity
- 26 units
- Agency-reported status
- Terminated
- Source record identifier
- Z-0650-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Model No. CP20120; Lot No. MS2117816; UDI No. (01)04048266150394(17)260706(10)MS2117816 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Domestic: Illinois; Foreign: Germany.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Feb 23, 2022
- Recall initiation date
- Jan 18, 2022
- Center classification date
- Feb 17, 2022
- Termination date
- Feb 16, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.