Home › Hovertech International › HoverSling
HoverSling
Hovertech International · Model HMSLING-50 · UDI-DI 00816299010657
5
510(k) clearances
38
Adverse events (5 deaths)
2
Recalls
57
Facilities
Description
50" Single Patient Use HoverSling
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-06-21 | Stryker Sustainability Solutions | 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 acros |
| 2005-09-13 | D.T. Davis Enterprises Ltd. | Instructions for use are not adhering to the product |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.