FDA Device recall Z-0650-2022
Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
- FDA Device
- Class II
- terminated
- Published 2022-02-23
On 2022-02-23 the FDA classified a Class II recall of Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only by Merete Medical, citing incorrect marketing label (25 mm) was applied to product size 20 mm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0650-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-01-18 |
| Published | 2022-02-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Merete Medical |
| Distribution | IL |
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.
Identifiers
| code_info | Model No. CP20120; Lot No. MS2117816; UDI No. (01)04048266150394(17)260706(10)MS2117816 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0650-2022%22
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