FDA Device recall Z-0987-2024

Flow-i C20 Anesthesia System, model 6677200

FDA Device
Class II
ongoing
Published 2024-02-14

On 2024-02-14 the FDA classified a Class II recall of Flow-i C20 Anesthesia System, model 6677200 by Getinge Usa Sales, citing potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0987-2024
Classification	Class II
Status	ongoing
Initiated	2023-12-11
Published	2024-02-14
Last updated	2026-09-13 11:57 UTC
Company	Getinge Usa Sales
Distribution	US

Product

Flow-i C20 Anesthesia System, model 6677200

Reason

Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.

Identifiers

code_info	UDI-DI: 07325710001349, Serial Numbers (US): 1202, 1224, 1281, 1282, 1545, 1546, 1651, 1657, 1786, 1787, 1860, 1861, 20… UDI-DI: 07325710001349, Serial Numbers (US): 1202, 1224, 1281, 1282, 1545, 1546, 1651, 1657, 1786, 1787, 1860, 1861, 2023, 2024, 2095, 2186, 2557, 2558, 2559, 2560, 2613, 2714, 2716, 2719, 2720, 2721, 2722, 2723, 2724, 2729, 2730, 2731, 2732, 2733, 2735, 2736, 2737, 2738, 2739, 2740, 2741, 2742, 2743, 2744, 2745, 2746, 2747, 2853, 2854, 2855, 2856, 2858, 2859, 2860, 2861, 2862, 2863, 2864, 2865, 2866, 2867, 2868, 2869, 4261, 4548, 4549, 4550, 5198, 5199, 5200, 5201, 5202, 5203, 5428, 5429, 5540, 5541, 5542, 5589, 5590, 5812, 5813, 5814, 5895, 6132, 6133, 6525, 6562, 6736, 6737, 6819, 6820, 6821, 6822, 6823, 6824, 6940, 7818, 7984, 7985, 7986, 7987, 7989, 7990, 7991, 7992, 7993, 7994, 8008, 8009, 8010, 8011, 8012, 8013, 8014, 8015, 8016, 8017, 8018, 8019, 8020, 8021, 8022, 8023, 8024, 8025, 8026, 8027.

code_info

UDI-DI: 07325710001349, Serial Numbers (US): 1202, 1224, 1281, 1282, 1545, 1546, 1651, 1657, 1786, 1787, 1860, 1861, 20…

UDI-DI: 07325710001349, Serial Numbers (US): 1202, 1224, 1281, 1282, 1545, 1546, 1651, 1657, 1786, 1787, 1860, 1861, 2023, 2024, 2095, 2186, 2557, 2558, 2559, 2560, 2613, 2714, 2716, 2719, 2720, 2721, 2722, 2723, 2724, 2729, 2730, 2731, 2732, 2733, 2735, 2736, 2737, 2738, 2739, 2740, 2741, 2742, 2743, 2744, 2745, 2746, 2747, 2853, 2854, 2855, 2856, 2858, 2859, 2860, 2861, 2862, 2863, 2864, 2865, 2866, 2867, 2868, 2869, 4261, 4548, 4549, 4550, 5198, 5199, 5200, 5201, 5202, 5203, 5428, 5429, 5540, 5541, 5542, 5589, 5590, 5812, 5813, 5814, 5895, 6132, 6133, 6525, 6562, 6736, 6737, 6819, 6820, 6821, 6822, 6823, 6824, 6940, 7818, 7984, 7985, 7986, 7987, 7989, 7990, 7991, 7992, 7993, 7994, 8008, 8009, 8010, 8011, 8012, 8013, 8014, 8015, 8016, 8017, 8018, 8019, 8020, 8021, 8022, 8023, 8024, 8025, 8026, 8027.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0987-2024%22

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