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MEDLINE STCVC2040BRecalls & reported problems

Medline Industries, Inc. · TRIPLE LUMEN CVC 20CM BUNDLE · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
1

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10653160372271), received between Feb 26, 2026 and Feb 26, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (1 report).

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

46 other recalls cover devices cleared under the same FDA submission (K213481); they may or may not involve this specific model.

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. May 21, 2026Open, Classified

    The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

    Z-2541-2026 · Root cause: Nonconforming Material/Component · FDA record ↗

Most reported problems

Device problems

  • Use of Device Problem1

Patient problems

  • Perforation of Vessels1

Recent adverse event reports

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

  • InjuryFeb 26, 2026Use of Device Problem

    ACCORDING TO THE CUSTOMER, WHILE A "RESIDENT" WAS PLACING A CVC LINE ON (B)(6) 2026 THEY "EXTRACTED THE GUIDEWIRE BACK THROUGH THE INTRODUCER NEEDLE" CAUSING THE GUIDEWIRE TO "FALL APART". THE CUSTOMER REPORTED THAT THE RESIDENT THEN "USED THE OTHER END OF THE GUIDEWIRE (BLUNT WITH NO J LOOP)" AND FED IT THROUGH THE INTRODUCER NEEDLE CAUSING THE GUIDEWIRE TO "PERFORATE THE PATIENT'S SUPERIOR VENA CAVA".

    Patient problems: Perforation of Vessels

    MAUDE report 24457758 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K213481. One submission often covers many models, so check the product and lot details in each record.

  • Z-3267-2026 · Aug 10, 2026 · Open, Classified
    Medline Convenience Kits: 1) MFC CRANIOTOMY PACK, Catalog Number: DYNJT8784; 2) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348Q; 3) SLUH CRANIOTOMY PACK-LF, Catalog Number:
  • Z-3229-2026 · Aug 10, 2026 · Open, Classified
    Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.
  • Z-3209-2026 · Jul 31, 2026 · Open, Classified
    Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A
  • Z-3137-2026 · Jul 23, 2026 · Open, Classified
    Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N
  • Z-3070-2026 · Jul 20, 2026 · Open, Classified
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 DRAWER #4 ACC010479A DRAWER
  • Z-3024-2026 · Jul 10, 2026 · Open, Classified
    Medline convenience kits labeled as: 1) MAJOR GYN PACK, Medline Kit SKU DYNJG001030C; 2) GYN LITHOTOMY PACK, Medline Kit SKU DYNJT8166; 3) OPEN HEART PACK, Medline Kit SKU DYNJ
  • Z-2995-2026 · Jul 8, 2026 · Open, Classified
    Medline medical convenience kits, labeled as: 1) CRANIOTOMY PACK, Medline Kit SKU DYNJT6545; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ88056A; 3) ENT SINUS PACK, Medline Kit SKU
  • Z-3054-2026 · Jun 12, 2026 · Open, Classified
    Medline Convenience Kits: 1) IV START KIT, Catalog Number: DYNDV2520; 2) PERIPHERAL LAB BLOOD CULTURE KIT, Catalog Number: DYNDH1983A; 3) PEDI EMERGENCY TRAY-PURPLE, Catalog Numb
  • Z-2736-2026 · Jun 10, 2026 · Open, Classified
    Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
  • Z-2764-2026 · Jun 8, 2026 · Open, Classified
    MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit SKU CDS984556N
  • Z-2749-2026 · Jun 5, 2026 · Open, Classified
    MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT, Medline Kit SKU DYKS1574A; 2) TOTAL KNEE BASIC, Medline Kit SKU DYNJ902378J; 3) TOTAL HIP, Medline Kit SKU DYNJ903492K;
  • Z-2748-2026 · Jun 5, 2026 · Open, Classified
    MEDLINE convenience kits labeled as: 1) C-SECTION, Medline SKU DYNJ910835; 2) C-SECTION, Medline SKU DYNJ910835A; medical convenience kits
  • Z-2747-2026 · Jun 5, 2026 · Open, Classified
    MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
  • Z-2697-2026 · May 28, 2026 · Open, Classified
    Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B;
  • Z-2611-2026 · May 28, 2026 · Open, Classified
    Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ909090B OPEN HEART CDS QVH CDS982523M

…and 31 more.

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.