FDA Device Intelligence
HomeINTERRAD MEDICAL, INC › SecurAcath

SecurAcath

INTERRAD MEDICAL, INC · Model 4F · UDI-DI 00865382000211

OKCLJSKMK Prescription
5
510(k) clearances
18
Adverse events
1
Recalls
2
Facilities

Recalls

DateFirmReason
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0

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.