Medshape, INC. recalls
Every recall we track for Medshape, INC. — 2 in all, from 2021–2025 — 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 Medshape, 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 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Medshape, 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 Medshape, INC. recalls
2 shown- Use cautionMedical device
Medshape, INC. recalls Medshape Universal Joints, REF: DNE-9000-UJ
Medshape recalls Universal Joints REF: DNE-9000-UJ due to potential pin dislodgement causing frame instability. Affected units include specific lots; contact for remedy.
MedshapeJun 2, 2025 - Lower riskMedical device
Medshape, INC. recalls DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Medshape recalls DYNANAIL MINI Endcap +6mm (Ref 2600-05-006) due to potential improper seating during procedures. This sterile medical device, sold with a prescription, may not seat flush with the nail, risking complications.
MedshapeNov 17, 2021
Medshape, INC. recall questions
How many recalls has Medshape, INC. had?
2 recalls from Medshape, INC. are on record with U.S. safety agencies, from 2021–2025.
What is the most recent Medshape, INC. recall?
Medshape, INC. recalls Medshape Universal Joints, REF: DNE-9000-UJ, dated Jun 2, 2025. Every Medshape, INC. recall is listed on this page, newest first.
What should I do if I have a recalled Medshape, 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 Medshape, 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.