Hazard

Mattress Defect recalls

13 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 13
Critical: 1
Severe: 11
Most recent: 2025-04-02

Of the 13 mattress defect recalls we have scored against our rubric, 1 (8%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 11 (85%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mattress defect recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–13 of 13

HighFDA (Devices)·Z-1468-2025·2025-04-02
Progressa bed surfaces recalled for mattress dips when head elevated
Baxter Healthcare's Progressa Bed Surfaces may develop dips in the mattress when the head of the bed is elevated, as air bladders inside can shift out of position. This could reduce the bed's effectiveness at preventing pressure ulcers.
Product
Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1152-2025·2025-02-26
Philips Allura Xper Patient Table Mattress Defect Fall Risk
Philips is recalling the Allura Xper FD10C patient examination table due to a mattress defect that may allow patients to fall from the table. The device was distributed worldwide.
Product
Allura Xper FD10C; Catalog number: 722001
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1156-2025·2025-02-26
Philips Azurion 5 M20 tables recalled due to patient fall risk
Philips is recalling Azurion 5 M20 imaging tables worldwide due to a mattress defect that could cause patients to fall from the table. This FDA Class I recall involves 632 units.
Product
Azurion 5 M20; Catalog numbers: (1) 722228, (2) 722232 (OUS ONLY), (3) 722281 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1147-2025·2025-02-26
Operating room table recalled due to mattress-related patient fall risk
Philips Allura Xper FD20 OR Table units (catalog numbers 722023, 722035) are recalled due to a mattress defect that could cause patients to fall during procedures.
Product
Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1157-2025·2025-02-26
Philips Azurion 7 B12 examination tables recalled due to patient fall risk
Philips Medical Systems is recalling Azurion 7 B12 examination tables due to a mattress-related patient fall risk. The recall affects 602 total units, including 94 in the US and 508 internationally.
Product
Azurion 7 B12; Catalog numbers: (1) 722067, (2) 722225, (3) 722235 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1149-2025·2025-02-26
Philips recalls Allura patient table mattress due to fall hazard
Philips is recalling Allura Xper patient table mattresses because a defect could cause patients to fall. The recall involves 302 units distributed globally.
Product
Allura Xper FD20/15; Catalog numbers: 722058
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1150-2025·2025-02-26
Philips Allura Xper FD20/20 Imaging Table Mattress Recall
Philips is recalling 114 units of the Allura Xper FD20/20 imaging table due to mattress defects that could cause patients to fall. 33 units are in the US; 81 are internationally distributed.
Product
Allura Xper FD20/20; Catalog numbers: 722038
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1155-2025·2025-02-26
Philips Azurion 5 M12 Patient Table Recalled for Fall Risk
Philips Medical Systems is recalling Azurion 5 M12 imaging tables due to a mattress defect that could allow patients to fall from the table.
Product
Azurion 5 M12; Catalog numbers: (1) 722227, (2) 722231 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1148-2025·2025-02-26
Philips Allura Xper FD20/10 Imaging System Patient Table Mattress Fall Risk
Philips is recalling the Allura Xper FD20/10 imaging system due to a defect in the patient table mattress that could allow patients to fall during procedures. The Class I recall affects 87 units distributed globally, including 22 in the US.
Product
Allura Xper FD20/10; Catalog numbers: 722029
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1158-2025·2025-02-26
Philips Azurion 7 B20 imaging system patient fall hazard from table mattress
Philips Azurion 7 B20 imaging systems are recalled because the patient table mattress may allow patients to fall. This FDA Class I recall affects 1,314 units distributed worldwide.
Product
Azurion 7 B20; Catalog numbers: (1) 722068, (2) 722226, (3) 722236.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1146-2025·2025-02-26
Surgical Operating Table Recalled Due to Patient Fall Risk
Philips Medical Systems is recalling the Allura Xper FD20 Biplane OR Table due to a mattress defect that could cause patients to fall during surgery. 3 units are affected globally.
Product
Allura Xper FD20 Biplane OR Table; Catalog numbers: (1) 722020, (2) 722025.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1154-2025·2025-02-26
Philips Azurion 3 M15 Patient Tables Recalled for Patient Fall Risk
Philips recalls Azurion 3 M15 imaging tables due to mattress defects that could cause patients to fall from the examination table.
Product
Azurion 3 M15; Catalog numbers: (1) 722064, (2) 722222 (3) 722280(OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1142-2025·2025-02-26
Medical imaging device patient table mattress may cause patient falls
Philips is recalling Allura Xper FD10 imaging devices because the patient table mattress may not securely hold patients during procedures, creating a fall hazard. The recall affects 2,274 units worldwide, including 459 in the U.S.
Product
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
Category
Medical Device
Distribution
Distributed nationwide