autoLog® ATLG110RRecalls & reported problems
Medtronic, Inc. · CONSOLE ATLG110R AUTOLOG 110 V REFURB · Class 2
Data updated Oct 18, 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 00673978521930), received between Nov 5, 2024 and Nov 5, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Mechanical Problem” (1 report).
1 other recall cover devices cleared under the same FDA submission (K972894); 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- 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.
MalfunctionNov 5, 2024Mechanical Problem; Mechanical Problem
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A AUTOLOG INSTRUMENT, IT WAS REPORTED THAT WHILE PROCESSING BLOOD IN A SURGERY CASE, THE UNIT SPILLED ALL OF ITS RED CELLS INTO THE WASTE BAG. PATIENT WAS NOT ABLE TO GET ANY OF THEIR BLOOD BACK. AUTOLOG OPERATOR STATED THAT THE UNIT NEVER SWITCHED TO WASH, AND PROCESSED ALL FLUIDS FROM RESERVOIR EMPTYING IT. CUSTOMER STATES THAT UNIT HAD PREVENTIVE MAINTENANCE IN 2021. USE OF INSTRUMENT WAS UNSPECIFIED. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT. CUSTOMER IS NOT REQUEST MEDTRONIC SERVICE NEEDS AT THIS TIME. NO FURTHER ACTION REQUIRED
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20611228 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K972894. One submission often covers many models, so check the product and lot details in each record.
- Z-1939-2010 · Apr 21, 2010 · TerminatedHospital Grade Power Cord, UL, Part # 66319, 055476, manufactured by Electri-Cord Manufacturing Co. beginning in February 2003. The cords are a detachable unit, supplied with the
Other APPARATUS, AUTOTRANSFUSION devices
- OASIS 3650-100Atrium Medical Corporation · APPARATUS, AUTOTRANSFUSION2 recalls22 reports
- EXPRESS 4050-100NAtrium Medical Corporation · APPARATUS, AUTOTRANSFUSION2 recalls2 reports
- NA ATL2001Medtronic, Inc. · APPARATUS, AUTOTRANSFUSION1 death79 reports
- autoLog IQ™ ATLGIQMedtronic, Inc. · APPARATUS, AUTOTRANSFUSION58 reports
- OCEAN 2050-000Atrium Medical Corporation · Apparatus, Autotransfusion1 recall2 reports
- NA BTC93Medtronic, Inc. · APPARATUS, AUTOTRANSFUSION1 recall2 reports
- NA BTC98Medtronic, Inc. · APPARATUS, AUTOTRANSFUSION1 recall0 reports
- HAEMONETICS CELL SAVER ELITE SYSTEM CSE-P-125Haemonetics Corporation · Apparatus, Autotransfusion47 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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