Epimed International, Inc. recalls
Every recall we track for Epimed International, Inc. — 3 in all, from 2019–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Epimed International, 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 | 2 | 0 | 2 |
| 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 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Epimed International, 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 Epimed International, Inc. recalls
2 shown- Lower riskMedical device
Epimed International, Inc. recalls Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural
Epimed recalls 19g x 24" epidural catheters (catalog #157-1924) due to potential coating cracking. Affected units have specific lot numbers. Contact for return instructions.
EpimedFeb 1, 2021 - Lower riskMedical device
Epimed International, Inc. recalls Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01)
Epimed recalls Versa Kath Mini Kit with mislabeled catheter size. The kit includes a 21-gauge catheter but labels state 12-gauge. This affects medical use for epidural anesthesia.
EpimedJun 18, 2019
Epimed International, Inc. recall questions
How many recalls has Epimed International, Inc. had?
3 recalls from Epimed International, Inc. are on record with U.S. safety agencies, from 2019–2021.
What is the most recent Epimed International, Inc. recall?
Epimed International, Inc. recalls Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural, dated Feb 1, 2021. Every Epimed International, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Epimed International, 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 Epimed International, 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.