Medline Industries, Inc. ECVC1525Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10653160334545), received between Jul 30, 2025 and Jul 30, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. May 15, 2023Open, Classified

   Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

   Z-2298-2023 · Root cause: Nonconforming Material/Component · FDA record ↗

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 30, 2025Retraction Problem; Detachment of Device or Device Component; No Flow

  EVENT 1 [DATE REDACTED] LOT: 2025030690: PLACEMENT OF CENTRAL LINE CATHETER - VANTEX CVC [CENTRAL VENOUS CATHETER] ANTIMICROBIAL 3 LUMEN, 7FR, 20CM, LOT #2025030690. SUCCESSFUL PLACEMENT OF CVC, CONFIRMED BY XR [X-RAY] TERMINATING IN THE SVC. BLOOD RETURN NOT PRESENT ON BLUE AND WHITE LUMEN, MINIMALLY PRESENT ON BROWN PORT WITH POSITIONING AND LAYING PATIENT SUPINE. EVENT 2 [DATE REDACTED] LOT: N/A: NO BLOOD RETURN FROM WHITE PORT OF TLC [TRIPLE LUMEN CATHETER] LINED PLACED [DATE REDACTED]. EVENT 3 [DATE REDACTED] LOT: 2025030690: VANTEX LEFT FEMORAL TLC INSERTED [DATE REDACTED]. NO BLOOD RETURN DOCUMENTED BY RN ON MEDIAL (BLUE) AND PROXIMAL (WHITE) PORTS. UPON ASSESSMENT THIS MORNING UNABLE TO DRAW BACK ON EITHER PORT BUT INFUSING WITH NO ISSUES. EVENT 4 [DATE REDACTED] LOT: 2025030690: VANTEX TLC INSERTION PER PROVIDER, NO BLOOD RETURN ON DISTAL BROWN PORT ON INSERTION PER PROVIDER AND NOTE. RN HAD NO BLOOD RETURN ON DISTAL BROWN PORT EITHER. PROVIDER ALSO NOTED DURING INSERTION THE NEEDLE FELL OFF THE SUTURE LINE. UNABLE TO FINISH NEEDED A SUPPLEMENTAL SUTURE KIT TO COMPLETE. EVENT 5 [DATE REDACTED] LOT: N/A: PATIENT HAD A RIGHT INTRAJUGULAR TRIPLE LUMEN CATHETER (TLC) THAT LOST

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22663921 ↗