N/A HM39SPU-BRecalls & reported problems

Stryker Sustainability Solutions, Inc. · HoverMatt 39" W x 78" L · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports: 0
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

Jun 21, 2023Class IIOpen, Classified
39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide mattresses, so there may be a decreased surface area available to distribute the patient's weight across, which may increase the effort exerted by staff for a lateral patient transfer, and there may be increased friction and shearing forces when the patient is moved resulting in skin tear injury.
Z-2394-2023 · Root cause: Packaging process control · Recall details · FDA record ↗

Device details

UDI-DI	`07613327487718`
Brand	N/A
Model	HM39SPU-B
Company	Stryker Sustainability Solutions, Inc.
Product code	FRZ · DEVICE, PATIENT TRANSFER, POWERED
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jul 21, 2025

Device type (GMDN): Inflatable patient transfer sliding mattress, single-use

An inflatable device designed to: 1) support a recumbent patient on a bed or table; and 2) assist healthcare professionals in the physical movement and transfer of a patient (e.g., hospitalized, disabled, geriatric) from one place to another using sliding techniques; some types may additionally be designed to provide skin protection to prevent pressure sores and/or support a patient in a specific position (e.g., Trendelenburg). It includes patient straps, handles for transfer, air hose inlets, and requires a pump (not included) for inflation; it is not intended for patient lifting. This is a single-use device.

Other DEVICE, PATIENT TRANSFER, POWERED devices

HoverMatt HM34HS
Hovertech International · DEVICE, PATIENT TRANSFER, POWERED
1 report
Single Patient Use HoverMatt HM39SPU-B
Hovertech International · DEVICE, PATIENT TRANSFER, POWERED
1 report

All DEVICE, PATIENT TRANSFER, POWERED devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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