Medical Device Recalls
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51 to 53 of 53 Results
Related Medical Device Recalls Recall Date to: 10/22/2014 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1776-2009 - Stryker dual 10.0 catheter set for PainPump2 and AutoFuser PainPump, sterile, Stryker Instruments, Kalamazoo, MI; REF 0537-210-000. | 2 | 08/19/2009 | Stryker Instruments Div. of Stryker Corporation |
Z-1777-2009 - Stryker dual 2.5 catheter set for PainPump2 and AutoFuser PainPump, sterile, Stryker Instruments, Kalamazoo, MI; REF 0537-225-000. | 2 | 08/19/2009 | Stryker Instruments Div. of Stryker Corporation |
Z-1771-2009 - Stryker standard catheter set for PainPump2 and AutoFuser PainPump, sterile, Stryker Instruments, Kalamazoo, MI; REF 0537-001-000. | 2 | 08/19/2009 | Stryker Instruments Div. of Stryker Corporation |
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