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Mullins X™

B BRAUN INTERVENTIONAL SYSTEMS, INC · Model 618808 · UDI-DI 04046964316432

DQY Prescription
10
510(k) clearances
41,518
Adverse events (903 deaths)
620
Recalls
276
Facilities

Description

MULLINS-X 18X3X12X8X100X.035 PTM448

Recalls

DateFirmReason
2026-04-30MICROVENTION INC.Due to an increase rate of balloon pinhole defects.
2026-04-21ARROW INTERNATIONAL, LLCLidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo
2025-09-25BALT USA, LLCDue to an identified manufacturing defect involving coating material lifting within the catheter's distal inner diameter/lumen.
2025-07-29Boston Scientific CorporationBoston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published l
2025-07-29Boston Scientific CorporationBoston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published l
2025-07-29Boston Scientific CorporationBoston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published l
2025-07-29Boston Scientific CorporationBoston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published l
2025-07-29Boston Scientific CorporationBoston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published l
2025-07-29Boston Scientific CorporationBoston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published l
2025-07-29Boston Scientific CorporationBoston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published l

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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.