FDA Device recall Z-1151-2025

Allura CV20

FDA Device
Class I
ongoing
Published 2025-02-26

On 2025-02-26 the FDA classified a Class I recall of Allura CV20 by Philips Medical Systems Nederland B V, citing possibility of the patient falling from the table related to the mattress used on the patient table.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1151-2025
Classification	Class I
Status	ongoing
Initiated	2025-01-13
Published	2025-02-26
Last updated	2026-09-13 11:57 UTC
Company	Philips Medical Systems Nederland B V
Distribution	US

Product

Allura CV20; Catalog numbers: 722031

Reason

Possibility of the patient falling from the table related to the mattress used on the patient table.

Identifiers

code_info	Catalog number: 722031; UDI-DI: no UDI; Serial Numbers: 155, 42, 13, 150, 87, 154, 29, 73, 88, 48, 109, 78, 53, 17, 63,… Catalog number: 722031; UDI-DI: no UDI; Serial Numbers: 155, 42, 13, 150, 87, 154, 29, 73, 88, 48, 109, 78, 53, 17, 63, 11, 97, 138, 86, 39, 36, 152, 135, 49, 18, 15, 91, 41, 20, 64, 9, 40, 55, 23, 71, 35, 33, 32, 30, 76, 70, 25, 133, 101, 128, 173, 124, 84, 92, 166, 26, 61, 130, 89, 90, 116, 117, 110, 111, 112, 113, 177, 164, 165, 161, 162, 163, 28, 100, 174, 167, 168, 119, 50, 24, 185, 126, 149, 147, 146, 140, 79, 127, 66, 137, 65, 38, 169, 121, 122, 123, 148, 184, 62, 170, 159, 125, 131, 151, 178, 181, 158, 157, 134, 46, 136, 96, 45, 180, 47, 99, 54, 115, 31, 175, 83, 77, 94, 85,

code_info

Catalog number: 722031; UDI-DI: no UDI; Serial Numbers: 155, 42, 13, 150, 87, 154, 29, 73, 88, 48, 109, 78, 53, 17, 63,…

Catalog number: 722031; UDI-DI: no UDI; Serial Numbers: 155, 42, 13, 150, 87, 154, 29, 73, 88, 48, 109, 78, 53, 17, 63, 11, 97, 138, 86, 39, 36, 152, 135, 49, 18, 15, 91, 41, 20, 64, 9, 40, 55, 23, 71, 35, 33, 32, 30, 76, 70, 25, 133, 101, 128, 173, 124, 84, 92, 166, 26, 61, 130, 89, 90, 116, 117, 110, 111, 112, 113, 177, 164, 165, 161, 162, 163, 28, 100, 174, 167, 168, 119, 50, 24, 185, 126, 149, 147, 146, 140, 79, 127, 66, 137, 65, 38, 169, 121, 122, 123, 148, 184, 62, 170, 159, 125, 131, 151, 178, 181, 158, 157, 134, 46, 136, 96, 45, 180, 47, 99, 54, 115, 31, 175, 83, 77, 94, 85,

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-1151-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.