FDA Device Intelligence
Home › ASPEN SURGICAL PRODUCTS, INC. › Cygnus

Cygnus

ASPEN SURGICAL PRODUCTS, INC. · Model DF100X · UDI-DI 10840113298638

JRJ Prescription
1
510(k) clearances
4
Adverse events
3
Recalls
24
Facilities

Description

AIRTIME™ DIRECTIONAL FLOW TUBING SET, 3 TUBING PORTS, 20 PER CASE

Recalls

DateFirmReason
2017-06-07Cenorin, LLCDryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.
2017-06-07Cenorin, LLCDryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.
2017-06-07Cenorin, LLCDryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.

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.