FDA Device Intelligence
Home › SEER MEDICAL HOLDINGS LIMITED › Seer Home

Seer Home

SEER MEDICAL HOLDINGS LIMITED · Model SM-01-9003-US · UDI-DI 09355751001099

PVP Prescription
0
510(k) clearances
0
Adverse events
1
Recalls
6
Facilities

Description

Take-home Kit

Recalls

DateFirmReason
2024-11-08Cardinal Health 200, LLCPotential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.

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.