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ACCEL®

B BRAUN INTERVENTIONAL SYSTEMS, INC · Model 612143 · UDI-DI 04046955237609

PXUOFL Prescription
0
510(k) clearances
15
Adverse events (2 deaths)
1
Recalls
20
Facilities

Description

3 PC INT, 018X60 SS-GOLD, 22GA CHIBA

Recalls

DateFirmReason
2024-06-11Merit Medical Systems, Inc.Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.