Terumo Medical Corporation: 9 recalls on record
Recalls filed with 1 agency: FDA (9).
First recall on record: July 3, 2013. Most recent: August 19, 2026.
Risk classification: Class I: 1 · Class II: 8
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| August 19, 2026 | FDA | GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The …Z-2930-2026 | Z-2930-2026 |
| July 31, 2019 | FDA | Terumo Sur-vet Needle, 20G x 1", Product Code 100204Z-1998-2019 | Z-1998-2019 |
| July 31, 2019 | FDA | Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280Z-2003-2019 | Z-2003-2019 |
| July 31, 2019 | FDA | Terumo Needle, 23G x 1", Product Code NN2325RZ-2005-2019 | Z-2005-2019 |
| June 5, 2019 | FDA | SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425, STFI-1435, …Z-1374-2019 | Z-1374-2019 |
| May 10, 2017 | FDA | Destination Renal Guiding Sheath Intended for the introduction of interventional and d…Z-2033-2017 | Z-2033-2017 |
| May 10, 2017 | FDA | SurFlo IV CatheterZ-1896-2017 | Z-1896-2017 |
| July 3, 2013 | FDA | Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut…Z-1611-2013 | Z-1611-2013 |
| July 3, 2013 | FDA | Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilit…Z-1612-2013 | Z-1612-2013 |
Questions about this company
- How many recalls does Terumo Medical Corporation have?
- Recalert has 9 U.S. recalls on record for Terumo Medical Corporation, published between July 3, 2013 and August 19, 2026.
- What was the most recent Terumo Medical Corporation recall?
- FDA recall Z-2930-2026, published August 19, 2026: GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.
- Which agencies have handled Terumo Medical Corporation recalls?
- Terumo Medical Corporation appears as the recalling firm in recalls from: FDA (9).
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