McKesson 419-64040Recalls & reported problems
Mckesson Medical-Surgical Inc. · BAG, EVA 2-PORT W/O LEGS 150ML(50/CS) · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10612479272122), received between Sep 10, 2025 and Sep 10, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (1 report).
17 other recalls cover devices cleared under the same FDA submission (K030888); 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Leak/Splash1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 10, 2025Leak/Splash; Mechanical Problem; Leak/Splash; Mechanical Problem
THE CUSTOMER REPORTED FIVE EVENTS OF LEAKING EVA 150 ML BAGS FROM A SINGLE LOT. LEAKS WERE IDENTIFIED BY CAREGIVERS AFTER PHARMACY FILLING BUT PRIOR TO PATIENT ADMINISTRATION. ONE REPORT DESCRIBED A HOLE IN THE BAG, ANOTHER DESCRIBED LEAKAGE ALONG THE SEAM, AND THE REMAINING LEAK LOCATIONS WERE NOT DISCLOSED. ALL PRODUCT SAMPLES WERE DISCARDED BY THE END USERS AND WERE NOT AVAILABLE FOR EVALUATION. AS THE LEAKS WERE DETECTED BEFORE ADMINISTRATION, THERE WAS NO PATIENT INVOLVEMENT OR HARM. NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23020536 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K030888. One submission often covers many models, so check the product and lot details in each record.
- Z-0330-2025 · Oct 9, 2024 · Open, ClassifiedVYGON 100 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9601; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0331-2025 · Oct 9, 2024 · Open, ClassifiedVYGON 250 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9602; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0332-2025 · Oct 9, 2024 · Open, ClassifiedCORMIX 150 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0344-2025 · Oct 9, 2024 · Open, ClassifiedImed Products Imed EVA BAG, 500 mL, 2-PORTS, REF IM68050; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0336-2025 · Oct 9, 2024 · Open, ClassifiedSECURE 100 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed), REF 66041; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0333-2025 · Oct 9, 2024 · Open, ClassifiedCORMIX 250 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0340-2025 · Oct 9, 2024 · Open, ClassifiedSECURE 500 mL EMPTY EVA CONTAINER With 2 Ports, REF 66050; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0341-2025 · Oct 9, 2024 · Open, ClassifiedSECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports, REF 66055; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0335-2025 · Oct 9, 2024 · Open, ClassifiedSECURE 100 mL EMPTY EVA CONTAINER With 2 Ports, REF 66040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0334-2025 · Oct 9, 2024 · Open, ClassifiedCORMIX 500 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64050; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0343-2025 · Oct 9, 2024 · Open, ClassifiedImed Products Imed EVA BAG, 250 mL, 2-PORTS, REF IM68045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0342-2025 · Oct 9, 2024 · Open, ClassifiedImed Products Imed EVA BAG, 150 mL, 2-PORTS, REF IM38040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0337-2025 · Oct 9, 2024 · Open, ClassifiedSECURE 50 mL EMPTY EVA CONTAINER With 2 Ports, REF 66042; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0338-2025 · Oct 9, 2024 · Open, ClassifiedSECURE 50 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed) , REF 66043; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
- Z-0339-2025 · Oct 9, 2024 · Open, ClassifiedSECURE 250 mL EMPTY EVA CONTAINER With 2 Ports, REF 66045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
…and 2 more.
Other Container, I.V. devices
- INTRAVIA 2B8011Baxter International Inc. · CONTAINER, I.V.127 reports
- INTRAVIA 2B8012Baxter International Inc. · CONTAINER, I.V.119 reports
- APEX™ 2112531B. Braun Medical Inc. · CONTAINER, I.V.69 reports
- APEX™ 2112530B. Braun Medical Inc. · CONTAINER, I.V.66 reports
- INTRAVIA 2B8013Baxter International Inc. · CONTAINER, I.V.64 reports
- SECURE® 66040Metrix Company, The · Container, I.V.1 recall8 reports
- MICROTEK 1Microtek Medical LLC · CONTAINER, I.V.1 recall8 reports
- SECURE® 66045Metrix Company, The · Container, I.V.1 recall7 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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