Merete Medical GmbH recalls
Every recall we track for Merete Medical GmbH — 5 in all, from 2020–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Merete Medical GmbH peaked in 2020 (4); 5 since 2017.
All FDA recall records for Merete Medical GmbH since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 4 | 0 | 4 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Merete Medical GmbH recalls
What to do if you have a recalled Merete Medical GmbH product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Merete Medical GmbH recalls
2 shown- Lower riskMedical device
Merete Medical GmbH recalls Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
Merete Medical recalls PediatrOS RigidTack size 20mm due to incorrect marketing label (25mm) applied. This affects products sold with the wrong size marking.
Merete MedicalJan 18, 2022 - Lower riskMedical device
Merete Medical GmbH recalls OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)
Merete Medical recalls OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails for tibia with mislabeling issues. Affected lots have specific use-by dates. Consumers should check their product labels.
Merete MedicalSep 18, 2020
Merete Medical GmbH recall questions
How many recalls has Merete Medical GmbH had?
5 recalls from Merete Medical GmbH are on record with U.S. safety agencies, from 2020–2022.
What is the most recent Merete Medical GmbH recall?
Merete Medical GmbH recalls Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only, dated Jan 18, 2022. Every Merete Medical GmbH recall is listed on this page, newest first.
Why are Merete Medical GmbH products recalled?
The most common reasons on record: Product may be mislabeled. (4).
What should I do if I have a recalled Merete Medical GmbH product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Merete Medical GmbH recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.