FDA Device Intelligence
HomeBiobase Biodustry(Shandong)Co., Ltd. › BIOBASE

BIOBASE

Biobase Biodustry(Shandong)Co., Ltd. · Model R1:60mL×5 R2:15mL×5 · UDI-DI 06936895301950

JGY
10
510(k) clearances
6
Adverse events
2
Recalls
27
Facilities

Recalls

DateFirmReason
2025-04-24Mckesson Medical-Surgical Inc. Corporate Officetransit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failur
2025-04-24Mckesson Medical-Surgical Inc. Corporate Officetransit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failur

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.