| CORDIS "Fire Star" 2.50 x 20 Dilatation Catheter, Catalog # 80120250, Distributed by Cordi recall (Z-0812-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 2.75 x 20 Dilatation Catheter, Catalog # 80120275, Distributed by Cordi recall (Z-0813-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 3.00 x 20 Dilatation Catheter, Catalog # 80120300, Distributed by Cordi recall (Z-0814-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 3.25 x 20 Dilatation Catheter, Catalog # 80120325, Distributed by Cordi recall (Z-0815-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 3.50 x 20 Dilatation Catheter, Catalog # 80120350, Distributed by Cordi recall (Z-0816-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 2.00 x 30, Dual Marker Band, Dilatation Catheter, Catalog # 8013020D, D recall (Z-0817-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 2.00 x 30, Single Marker Band, Dilatation Catheter, Catalog # 8013020S, recall (Z-0818-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 2.25 x 30 Dilatation Catheter, Catalog # 80130225, Distributed by Cordi recall (Z-0819-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 2.50 x 30 Dilatation Catheter, Catalog # 80130250, Distributed by Cordi recall (Z-0820-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 2.75 x 30 Dilatation Catheter, Catalog # 80130275, Distributed by Cordi recall (Z-0821-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 3.00 x 30 Dilatation Catheter, Catalog # 80130300, Distributed by Cordi recall (Z-0822-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 3.25 x 30 Dilatation Catheter, Catalog # 80130325, Distributed by Cordi recall (Z-0823-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS "Fire Star" 3.50 x 30 Dilatation Catheter, Catalog # 80130350, Distributed by Cordi recall (Z-0824-2008) | Cordis Corporation | 2008-02-06 |
| CORDIS SV-5 Steerable Guidewire, 180 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson recall (Z-1492-06) | Cordis Corporation | 2006-09-09 |
| CORDIS-SV-5 Steerable Guidewire, 300 cm.,5 Steerable Guidewires,Cordis a Johnson Johnson C recall (Z-1493-06) | Cordis Corporation | 2006-09-09 |
| CORDIS SV-8 Steerable Guidewire, 180 cm. , 5 Steerable Guidewires, Cordis a Johnson Johnso recall (Z-1494-06) | Cordis Corporation | 2006-09-09 |
| CORDIS SV-8 Steerable Guidewire, 300 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson recall (Z-1495-06) | Cordis Corporation | 2006-09-09 |
| Cordis INFINITI 6 French Diagnostic Catheter. Catalog 534-6xxT. That is: 534614T, 534615T, recall (Z-1240-06) | Cordis Corporation | 2006-07-13 |
| Product is a Powerflex P3 Dialation Catheter. Product is labeled in part: ''***POWERFLEX P recall (Z-1556-05) | Cordis Corporation | 2005-09-21 |
| Vistabritetip IG Introducer, Introducer Guide. Labeled as sterile, sterilized with ethylen recall (Z-0588-05) | Cordis Corporation | 2005-03-10 |
| Cypher Sirolimus-eluting Coronary Stent on Raptor Over-the-Wire Delivery System (CWSxxxxx) recall (Z-0555-05) | Cordis Corporation | 2005-02-18 |
| VISTA BRITE TIP RDC(1) Guiding Catheter. Product Code 67021055, lot X0704002, Precutaneous recall (Z-0434-05) | Cordis Corporation | 2005-01-26 |
| Polymeric coated stent. Cypher BX Velocity Cardio Sirolimus Stents. recall (Z-0437-05) | Cordis Corporation | 2005-01-26 |
| CordisEndomyocardial Biopsy Forceps 7F 104 cm Standard, Product Number 504300L recall (Z-0564-04) | Cordis Corporation | 2004-07-20 |
| Cordis Biopsy Forceps 7F 104 cm Standard, Product Number 504300L recall (Z-0565-04) | Cordis Corporation | 2004-07-20 |
| The device is in a tyvek pouch and is labeled in part: Aviator Peripheral Dilatation Cathe recall (Z-0566-04) | Cordis Corporation | 2004-07-20 |
| This device is labeled as Sterile and is packaged in a Tyvek pouch with the following labe recall (Z-0567-04) | Cordis Corporation | 2004-07-20 |
| This medical device is packaged in an inner Tyvek pouch and then in an outer carton. The o recall (Z-0909-04) | Cordis Corporation | 2004-07-20 |
| Product is Cordis Brite Tip Catheter Sheath Introducer (4, 7, 8, 9, 10 and 11French sizes recall (Z-0941-03) | Cordis Corporation | 2003-06-12 |
| The device is Labeled as SMART Control TRANSHEPATIC BILIARY STENT REF (PRODUCT NUMBER LIST recall (Z-0707-03) | Cordis Corporation | 2003-04-02 |
| Product is packaged and labeled as: ''Cordis PRECISE Nitinol Stent Transhepatic Billiary S recall (Z-0323-03) | Cordis Corporation | 2002-12-05 |