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
Recalls naming this device
- 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, ClassifiedMedline 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, ClassifiedMedline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.
- Z-3209-2026 · Jul 31, 2026 · Open, ClassifiedConvenience kits MYRINGOTOMY PACK-LF DYNJ59097A
- Z-3137-2026 · Jul 23, 2026 · Open, ClassifiedMedline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N
- Z-3070-2026 · Jul 20, 2026 · Open, ClassifiedMedline 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, ClassifiedMedline 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, ClassifiedMedline 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, ClassifiedMedline 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, ClassifiedMedline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
- Z-2764-2026 · Jun 8, 2026 · Open, ClassifiedMEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit SKU CDS984556N
- Z-2749-2026 · Jun 5, 2026 · Open, ClassifiedMEDLINE 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, ClassifiedMEDLINE 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, ClassifiedMEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
- Z-2697-2026 · May 28, 2026 · Open, ClassifiedMedline 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, ClassifiedMedline 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.