Oscor, Inc. recalls

38 recalls on record · latest: December 22, 2021

Official U.S. recall history for Oscor, Inc., compiled from official government records.

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Oscor Inc. recalls Destino Twist 14F (also branded as Guidestar 14F)

December 22, 2021 · Medical device recalls Moderate risk There is potential for separation between the threaded hub and threaded cap at…

Oscor, Inc. recalls AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various typ…

March 10, 2021 · Medical device recalls Moderate risk Potential for open seal on sterile product

Oscor Inc. recalls Oscor — Temporary Bipolar Pacing Lead, Model TB

November 12, 2018 · Drug & medication recalls Connector cap housing may slide and potentially expose the connection wire — De…

Oscor Inc. recalls Oscor — Temporary Bipolar Pacing Leads

September 27, 2018 · Medical device recalls The connector cap housing may slide and potentially expose the connection wire…

Oscor, Inc. recalls TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right He…

September 26, 2018 · Medical device recalls High risk During the use of some TB - Temporary Bipolar Pacing Leads, featuring the 2mm u…

Oscor, Inc. recalls ATAR — Extension cable

July 6, 2017 · Medical device recalls Cable separating from the connector at the proximal end — Defect

Oscor, Inc. recalls ATAR Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 53912 Disposable Series, and XI D…

March 31, 2017 · Medical device recalls High risk The Reusable Oscor ATAR extension cables could separate from the connector duri…

Oscor, Inc. recalls ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusabl…

March 31, 2017 · Medical device recalls High risk The Reusable Oscor ATAR extension cables could separate from the connector duri…

Oscor, Inc. recalls OSCOR ADELANTE BREEZWAY 10F STRAIGHT S79CM D84CM Catalog # AB101219 Is designed to facilitate the introduction of cathe…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S79CM D84CM GLOBAL Catalog # 990079-090-000 Is designed to facilit…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL Catalog # 990061-090-000 Is designed to facilit…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F C90¿ S79CM D84CM Catalog # AB101078 Is designed to facilitate the introduction of catheter…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C70¿ S61CM D66CM GLOBAL Catalog # 990061-070-000 Is designed to facilit…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZWAY 8F STRAIGHT S79CM D84CM Catalog # AB081211 Is designed to facilitate the introduction of cathet…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F C55¿ S79CM D84CM Catalog # AB101076 Is designed to facilitate the introduction of catheter…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F C70¿ S61CM D66CM Catalog # AB101073 Is designed to facilitate the introduction of catheter…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C55¿ S79CM D84CM GLOBAL Catalog # 990079-055-000 Is designed to facilit…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C55¿ S61CM D66CM GLOBALCatalog # 990061-055-000 Is designed to facilita…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C90¿ S61CM D66CM Catalog # AB081042 Is designed to facilitate the introduction of catheters…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C55¿ S61CM D66CM Catalog # AB081040 Is designed to facilitate the introduction of catheters…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F STRAIGHT S61CM D66CM Catalog # AB081210 Is designed to facilitate the introduction of cathe…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C120¿ S61CM D66CM GLOBAL Catalog # 990061-120-000 Is designed to facili…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB101218 Is designed to facilitate the introduction of cath…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C55¿ S79CM D84CM Catalog # AB081044 Is designed to facilitate the introduction of catheters…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F C70¿ S79CM D84CM Catalog # AB101077 Is designed to facilitate the introduction of catheter…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C55¿ S61CM D66CM GLOBAL Catalog # 990061-055-000 Is designed to facilit…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C70¿ S79CM D84CM GLOBAL Catalog # 990079-070-000 Is designed to facilit…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR BREEZEWAY 10F S60.8CM D65.6CM FIRM TIP Catalog # AB1061FT Is designed to facilitate the introduction of catheters…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL Catalog # 990061-090-000 Is designed to facilit…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F C55¿ S61CM D66CM Catalog # AB101072 Is designed to facilitate the introduction of catheter…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F C120¿ S61CM D66CM Catalog # AB101075 Is designed to facilitate the introduction of cathete…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F C120¿ S79CM D84CM Catalog # AB101078 Is designed to facilitate the introduction of cathete…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C70¿ S61CM D66CM Catalog # AB081041 Is designed to facilitate the introduction of catheters…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C120¿ S79CM D84CM Catalog # AB081047 Is designed to facilitate the introduction of catheter…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB10218 Is designed to facilitate the introduction of cathe…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C90¿ S79CM D84CM Catalog # AB081046 Is designed to facilitate the introduction of catheters…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C120¿ S61CM D66CM Catalog # AB081043 Is designed to facilitate the introduction of catheter…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…

Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C70¿ S79CM D84CM Catalog # AB081045 Is designed to facilitate the introduction of catheters…

October 5, 2016 · Medical device recalls Moderate risk Complaint that during insertion of the dilator through the sheath a fragment of…