Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K020715 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED, Model 861304, HSI code... | 2 | 02/19/2020 | Philips North America LLC |
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758 | 2 | 09/20/2019 | Philips North America LLC |
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