Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K153702 |
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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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Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider E... | 2 | 04/25/2024 | Philips North America Llc |
Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PI... | 2 | 03/27/2024 | Philips North America |
(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model... | 2 | 01/13/2024 | Philips North America |
(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436 | 2 | 01/13/2024 | Philips North America |
Patient Information Center iX with Software Version Number 4.x in the following: (1) Patient Info... | 2 | 09/19/2023 | Philips North America Llc |
Philips Patient Information Center iX configured with a regional setting which uses a comma for a de... | 3 | 06/12/2019 | Philips North America, LLC |
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