Terumo Medical Corporation recalls
Every recall we track for Terumo Medical Corporation — 14 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Terumo Medical Corporation peaked in 2019 (12); 14 since 2017.
All FDA recall records for Terumo Medical Corporation 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 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 12 | 0 | 12 |
| 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 | 1 | 0 | 1 |
What to do if you have a recalled Terumo Medical Corporation 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 Terumo Medical Corporation recalls
4 shown- Lower riskMedical device
Terumo Medical Corporation recalls GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to
Terumo recalls 5 units per box of Glidesheath Slender A-Kit 6F 10CM (Product Code 60-1060) due to incorrect 0.025 guidewire packaging. This may cause catheter placement issues during medical procedures.
TerumoJun 15, 2026 - Lower riskMedical device
Terumo Medical Corporation recalls SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425, STFI-1435, STFI-1625, STFI-1635, STFI-1825,
Terumo recalls SOLOPATH Balloon Expandable TransFemoral Systems (models STFI-1425 to STFI-2135) due to potential tip dislodgement from the sheath, which could cause loss of smooth transition during vascular procedures.
TerumoApr 26, 2019 - Lower riskMedical device
Terumo Medical Corporation recalls Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280
Terumo recalls 25G x 5/8" Sur-vet Needles (Product Code 100280) due to potential loss of sterility. Affected lot numbers: 180814C, 181002C, 181009C.
TerumoFeb 8, 2019 - Lower riskMedical device
Terumo Medical Corporation recalls Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath is
Terumo recalls Destination Guiding Sheath catheter introducers with catalog number RSR06 that may have tucking depth marginally outside specifications. This could affect medical procedures.
TerumoSep 12, 2017
Terumo Medical Corporation recall questions
How many recalls has Terumo Medical Corporation had?
14 recalls from Terumo Medical Corporation are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Terumo Medical Corporation recall?
Terumo Medical Corporation recalls GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to, dated Jun 15, 2026. Every Terumo Medical Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Terumo Medical Corporation 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 Terumo Medical Corporation 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.