HoverMatt recall
HoverMatt, 39" W x 78" L, REF: HM39SPU-B
Why was HoverMatt recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 07613327487718, Lot: 0000185127, Distribution Dates: 11/28/2022-12/08/2022
- Product
- HoverMatt, 39" W x 78" L, REF: HM39SPU-B
- Recalling firm
- Stryker Sustainability Solutions
- Quantity
- 340
- Distribution
- US: WI, ID, CA, FL, HI, MD, RI, AZ, MA, GA, IL
- Recall date
- August 16, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)