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 month

Severity split

Class I 6 15%Class II 33 85%Class III 0 0%

By year

Ongoing oscor recalls

3 active

All oscor recalls, newest first

39 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IAbiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel recalledOscorPackaging DefectsMA
DeviceCLASS IAbiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel recalledOscorPackaging DefectsMA
DeviceCLASS IAbiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel recalledOscorPackaging DefectsMA
DeviceCLASS IIDestino Twist 14F (also branded as Guidestar 14F) recalled by OscorOscorOtherPA, TN
DeviceCLASS IIAngioDynamics SafeSheath Ultralite 10F recalled by OscorOscorSterilityNationwide
DeviceCLASS ITB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F recalled by OscorOscorDevice MalfunctionNationwide
DeviceCLASS IAtar Reusable Extension Cable, sold under brand names recalled by Oscorsold underOscorOther40 states
DeviceCLASS IAtar Disposable Extension Cable, sold under brand names recalledsold underOscorOther40 states
DeviceCLASS IIAdelante Breezeway 8f C70¿ S79cm D84cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f C120¿ S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f C90¿ S79cm D84cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 10f Straight S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f C120¿ S79cm D84cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f C70¿ S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 10f C120¿ S79cm D84cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 10f C120¿ S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 10f C55¿ S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIMedtronic Arrive Braided Transseptal Sheath 10f C90¿ S61cm recalledOscorOther8 states
DeviceCLASS IIBreezeway 10f S60 recalled by OscorOscorOther8 states
DeviceCLASS IIMedtronic Arrive Braided Transseptal Sheath 10f C70¿ S79cm recalledOscorOther8 states
DeviceCLASS IIMedtronic Arrive Braided Transseptal Sheath 10f C55¿ S61cm recalledOscorOther8 states
DeviceCLASS IIAdelante Breezeway 10f C70¿ S79cm D84cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f C55¿ S79cm D84cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 10f Straight S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIMedtronic Arrive Braided Transseptal Sheath 10f C120¿ recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f Straight S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f C55¿ S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIAdelante Breezeway 8f C90¿ S61cm D66cm recalled by OscorOscorOther8 states
DeviceCLASS IIMedtronic Arrive Braided Transseptal Sheath 10F C55¿ S61CM recalledOscorOther8 states
DeviceCLASS IIMedtronic Arrive Braided Transseptal Sheath 10f C55¿ S79cm recalledOscorOther8 states

About 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.