FDA Device Intelligence
Home › TELEFLEX INCORPORATED › QUIKCLOT

QUIKCLOT

TELEFLEX INCORPORATED · Model 4040 · UDI-DI 10841495149686

POD Prescription
6
510(k) clearances
6
Adverse events
1
Recalls
15
Facilities

Recalls

DateFirmReason
2021-10-14Beeken Biomedical, LLCEndotoxin levels exceeded allowable limits.

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.