FDA Device Intelligence
Home › Cardinal Health, Inc. › NOVAPLUS

NOVAPLUS

Cardinal Health, Inc. · Model V7059A · UDI-DI 10884521743533

KME
10
510(k) clearances
94
Adverse events
2
Recalls
589
Facilities

Description

Underpad Ultra Extra Heavy

Recalls

DateFirmReason
2023-06-23Microtek Medical Inc.Certain lots of the products have a Naphthalene odor.
2017-12-27LITTLE RAPIDS CORPORATIONThe secondary supplier provided material was within specification but did not meet our design needs compared to the primary manufacturer. The product is designed for patient trans

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 docs
Data 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.