Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K973486 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| FASTPAK batteries labeled Manufactured for Medtronic Physio-Control 11811 Willows Rd, Redmond, WA U... | 2 | 08/24/2008 | Physio Control, Inc. |
| LIFEPAK 12 defibrillator/monitor is a portable, battery operated, complete acute cardiac care respon... | 2 | 02/05/2003 | Medtronic Physio Control Corp |
| 12-lead ECG Cable Assembly contains the following cable and attachments: Main Cable with Limb Lea... | 3 | 06/22/2011 | Physio Control, Inc. |
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