Medical Device Recalls
-
71 to 72 of 72 Results
510(K) Number: K043466 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Stryker 2.5 catheter set for PainPump2 and AutoFuser PainPump, sterile, Stryker Instruments, Kalamaz... | 2 | 08/19/2009 | Stryker Instruments Div. of Stryker Corporation |
Stryker 10.0 catheter set for PainPump2 and AutoFuser PainPump, sterile, Stryker Instruments, Kalama... | 2 | 08/19/2009 | Stryker Instruments Div. of Stryker Corporation |
-