Oscor Inc. recalls
Every recall we track for Oscor Inc. — 6 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
6 recalls since 2017. 17% rated “stop using now”.
All FDA recall records for Oscor 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 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 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) | 1 | 0 | 2 | 0 | 3 |
What to do if you have a recalled Oscor 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 Oscor Inc. recalls
4 shown- Lower riskMedical device
Oscor Inc. recalls Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F
Oscor recalls Abiomed 14F Introducer Kits with potential leaks in sheaths. Affected kits have specific lot numbers and may require replacement.
OscorJun 10, 2026 - Lower riskMedical device
Oscor Inc. recalls Destino Twist 14F (also branded as Guidestar 14F)
Oscor recalls Destino Twist 14F (Guidestar 14F) models with possible hub separation risk. Affected units include specific model numbers and lots. No remedy stated in recall.
OscorDec 22, 2021 - Lower riskMedical device
Oscor, Inc. recalls AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various
Oscor recalls AngioDynamics SafeSheath ULTRALITE 10:10F model VI10 due to potential open seal on sterile product. This could compromise sterility during medical procedures.
OscorMar 10, 2021 - Lower riskMedical device
Oscor, Inc. recalls TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right
Oscor recalls TB Series Bipolar Pacing Leads with 2mm unshrouded connectors for potential connector cap sliding, risking wire breakage during movement.
OscorSep 26, 2018
Oscor Inc. recall questions
How many recalls has Oscor Inc. had?
6 recalls from Oscor Inc. are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Oscor Inc. recall?
Oscor Inc. recalls Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F, dated Jun 10, 2026. Every Oscor Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Oscor 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 Oscor 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.