Oscor recalls
Oscor has 39 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 22 Jul 2026. 3 are still ongoing. 3 were reported in the last 12 months.
Total recalls39since 2012
Last 12 months3reported
Class I615% of total
Ongoing3latest 22 Jul 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 6 15%Class II 33 85%Class III 0 0%
Why oscor is recalled
Product types
By year
Ongoing oscor recalls
3 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel recalled | Oscor | Packaging Defects | MA |
| Device | CLASS I | Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel recalled | Oscor | Packaging Defects | MA |
| Device | CLASS I | Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel recalled | Oscor | Packaging Defects | MA |
All oscor recalls, newest first
39 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.