Medical Device Recalls
-
1 to 2 of 2 Results
Related Medical Device Recalls |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Z-0017-2011 - Guidant, Vitality HE ICD, Model: T180DDR, Sterile Lot, Guidant Corporation, Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798. | 2 | 10/07/2010 | Boston Scientific CRM Corp |
Z-0016-2011 - Guidant, CONTAK RENEWAL 3/3RF Models H170, H175, H177, H179, H210, H215, H217, H219, Guidant Corporation, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 CONTAK RENEWAL 4/4RF Models H190*, H19... | 2 | 10/07/2010 | Boston Scientific CRM Corp |
-