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

NOVAPLUS

Cardinal Health, Inc. · Model VP3036C · UDI-DI 10884521743403

KME
10
510(k) clearances
69
Adverse events
2
Recalls
584
Facilities

Description

Premium Comfort Underpad Maximum

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.