Uromedica Inc. recalls
Every recall we track for Uromedica Inc. — 2 in all, from 2019–2021 — 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 Uromedica 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 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 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 Uromedica 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 Uromedica Inc. recalls
2 shown- Use cautionMedical device
Uromedica Inc. recalls UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.
Uromedica recalls specific implantation instrument sets (REF 750041) due to potential damage to ProACT devices during surgery. Affected units have lot numbers UM00794 or UM00817.
UromedicaNov 22, 2021 - Lower riskMedical device
Uromedica Inc. recalls ProACT Implantation Instrument Set, is a reusable, steam sterilizable surgical instrument set consisting of a U-Channel
Uromedica recalls ProACT Implantation Instrument Set (Model 750041, Lot UM00650) due to potential U-channel sheath damage to implant devices during use. Affected units may cause device damage when passed through sheaths.
Uromed: ProACTApr 10, 2019
Uromedica Inc. recall questions
How many recalls has Uromedica Inc. had?
2 recalls from Uromedica Inc. are on record with U.S. safety agencies, from 2019–2021.
What is the most recent Uromedica Inc. recall?
Uromedica Inc. recalls UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile., dated Nov 22, 2021. Every Uromedica Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Uromedica 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 Uromedica 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.