Oscor Recalls
39 recalls on record · November 7, 2012 to July 22, 2026 · Medical Devices
Recalls by year
12
16
17
18
21
22
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C120¿ S79CM D84CM Catalog # AB081047 Is designed to facilitate the introduction of cathet
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C90¿ S79CM D84CM Catalog # AB081046 Is designed to facilitate the introduction of catheters
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C70¿ S79CM D84CM Catalog # AB081045 Is designed to facilitate the introduction of catheter
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C55¿ S79CM D84CM Catalog # AB081044 Is designed to facilitate the introduction of catheter
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C120¿ S61CM D66CM Catalog # AB081043 Is designed to facilitate the introduction of cathet
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C90¿ S61CM D66CM Catalog # AB081042 Is designed to facilitate the introduction of catheter
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C70¿ S61CM D66CM Catalog # AB081041 Is designed to facilitate the introduction of catheter
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
December 28, 2016Medical DevicesFDA
Oscor, Inc. recalls OSCOR ADELANTE BREEZEWAY 8F C55¿ S61CM D66CM Catalog # AB081040 Is designed to facilitate the introduction of catheter
Hazard: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
November 7, 2012Medical DevicesFDA
Oscor, Inc. recalls Myocardial Heart Wires Intended for temporary atrial and ventricular pacing and sensing during or after cardiac surge
Hazard: Oscor, Inc. in Palm Harbor, FL is recalling myocardial heart wires, models TME60S, TME64S, TME64C, TME64S-3, TME65S, and TME66S. The recall was initiated due to the spacing between anchoring zig-zag to electrode is out of specification.