Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 04/18/2015 510(K) Number: K052465 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P and 350P device (SAM 300P and ... | 2 | 07/24/2014 | Heartsine Technologies, Limited |
HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A0003500... | 1 | 10/27/2012 | Heartsine Technologies, Limited |
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