Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-1772-2019 - Philips IntelliBridge System configured with a regional setting which uses a comma for a decimal separator: 866417 IntelliBridge System C.01 (or later) 866418 IntelliBridge System C.01 upgrade (or... | 3 | 06/12/2019 |
FEI # 1218950 Philips North America, LLC |
| Z-1771-2019 - Philips Patient Information Center iX configured with a regional setting which uses a comma for a decimal separator: 866389 Patient Information Center iX B.01 (or later); 866390 Patient Information ... | 3 | 06/12/2019 |
FEI # 1218950 Philips North America, LLC |
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