autoLog® ATLG110 (UDI 00643169201347)Recalls & reported problems
Medtronic, Inc. · CONSOLE ATLG110 AUTOLOG SYS ENGLISH · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00643169201347), received between Sep 9, 2024 and Feb 18, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).
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
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
- Fluid/Blood Leak1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2025Fluid/Blood Leak; Fluid/Blood Leak
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF AN AUTOLOG INSTRUMENT, IT WAS REPORTED A BOWL SPILL. THE INSTRUMENT WAS REPLACED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THERE WAS NO TRANSFUSION REQUIRED. BIOMED HAD NO ADDITIONAL INFORMATION ABOUT DEVICE, ONLY THAT IT HAD A BLOOD LEAK. THE TECHNICIAN ASSUMED BLOOD LEAKED THROUGH THE BOWL AS THIS IS ONLY WAY A VISIBLE LEAK OCCURS.
Patient problems: Hemorrhage/Blood Loss/Bleeding; No Clinical Signs, Symptoms or Conditions
MAUDE report 21395831 ↗MalfunctionSep 9, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF AN AUTOLOG INSTRUMENT, IT WAS REPORTED THAT THE INSTRUMENT WAS NOT SENDING THE CORRECT AMOUNT OF BLOOD TO BAG OR WASTE. THE INSTRUMENT WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE BLOOD WAS SENT TO THE WASTE BAG. THERE IS NO INFO ON THE AMOUNT OF BLOOD, BUT A TRANSFUSION WAS NOT REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20169886 ↗
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- OCEAN 2050-000Atrium Medical Corporation · Apparatus, Autotransfusion1 recall2 reports
- NA BTC98Medtronic, Inc. · APPARATUS, AUTOTRANSFUSION1 recall0 reports
- HAEMONETICS CELL SAVER ELITE SYSTEM CSE-P-125Haemonetics Corporation · Apparatus, Autotransfusion47 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.