Amendia, Inc recalls
Every recall we track for Amendia, Inc — 2 in all, all from 2017 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Amendia, Inc 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 | 2 | 0 | 2 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 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 |
What to do if you have a recalled Amendia, Inc 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 Amendia, Inc recalls
2 shown- Lower riskMedical device
Amendia, Inc recalls Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws are self-drilling variable screws that are intended to
Amendia recalls Ceres Self-Drilling Variable Screws 4.0 x 12mm due to incorrect length marking (some screws are 14mm instead of 12mm).
AmendiaJul 7, 2017 - Lower riskMedical device
Amendia, Inc recalls Mac Pin Non-Cannulated Screw, 6.5 x 60mm
Amendia recalls Mac Pin Non-Cannulated Screws (6.5 x 60mm) due to incorrect labeling of pin length. This may cause improper use in medical applications.
AmendiaJul 7, 2017
Amendia, Inc recall questions
How many recalls has Amendia, Inc had?
2 recalls from Amendia, Inc are on record with U.S. safety agencies, from 2017.
What is the most recent Amendia, Inc recall?
Amendia, Inc recalls Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws are self-drilling variable screws that are intended to, dated Jul 7, 2017. Every Amendia, Inc recall is listed on this page, newest first.
What should I do if I have a recalled Amendia, Inc 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 Amendia, Inc 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.