SECURE® 66041Recalls & reported problems
Metrix Company, The · EMPTY EVA CONTAINER With 2 Ports (Bulk Packed) · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 50812496011553), received between Apr 26, 2024 and Oct 3, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
16 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Oct 9, 2024Open, Classified
A limited number of IV bags have been found to leak during filling.
Z-0336-2025 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Contamination /Decontamination Problem1
- Fluid/Blood Leak1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 3, 2024Fluid/Blood Leak; Mechanical Problem; Fluid/Blood Leak; Mechanical Problem
THE CUSTOMER STATED "IT APPEARS THAT THE BAG ITSELF ISN'T SEALED TO THE PORT IN SOME CASES. ONE OTHER INTERESTING THING THAT WE HAVE NOTICED - ALL THE BAGS THAT ARE LEAKING HAVE A SMALL NUMBER 6 IMPRINTED ON THE BAG ITSELF". 15 SAMPLES WERE IDENTIFIED FOR LEAKING BY THE PHARMACY DURING THE COMPOUNDING PROCESS. THERE WAS NO PATIENT INVOLVEMENT FOR THIS EVENT. SAMPLES FROM WITHIN THE LOT WERE RETURNED FOR INVESTIGATION. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20360443 ↗MalfunctionApr 26, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem
THE CUSTOMER REPORTED THAT ONE SAMPLE OF PRODUCT WAS IDENTIFIED WITH "A PORT THAT APPEARS TO BE CONTAMINATED OR DAMAGED". THE CUSTOMER REPORTED THE CONTAMINATION APPEARED TO BE STREAKS DOWN THE SIDE OF THE PORT. THIS WAS NOTED BY THE PHARMACY DURING COMPOUNDING. THE SAMPLE WAS RETURNED FOR EVALUATION. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19192257 ↗
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-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-0345-2025 · Oct 9, 2024 · Open, ClassifiedImed Products Imed EVA BAG, 1000 mL, 2-PORTS, REF IM68055; 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-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-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-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-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.
- 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-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-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-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-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-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-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-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.
…and 1 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.