Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0116-06 - QUIK-COMBO pacing/defibrillation/ECG (therapy) cables used with the LIFEPAK 12 defibrillator/monitor series. | 2 | 11/02/2005 |
FEI # 3015876 Medtronic Emergency Response Systems, Inc. |
| Z-0117-06 - standard (hard) paddles used with the LIFEPAK 12 defibrillator/monitor series. | 2 | 11/02/2005 |
FEI # 3015876 Medtronic Emergency Response Systems, Inc. |
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