autoLog® ATLG110 (UDI 00613994667670)Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00613994667670), received between Aug 23, 2024 and Jul 24, 2025 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (3 reports).

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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 24, 2025Mechanical Problem; Mechanical Problem

  MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF AN AUTOLOG INSTRUMENT, IT WAS REPORTED THAT THE SYSTEM IS SENDING THE SAMPLES TO THE WASTE INSTEAD OF TO THE COLLECTION TANK. USE OF INSTRUMENT WAS UNSPECIFIED. THERE WAS NO PATIENT INVOLVEMENT, SO NO ADVERSE EFFECT OCCURRED. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE CUSTOMER WOULD NOT BE MOVING FORWARD WITH THE REPAIR ON THEIR LEGACY AUTOLOG UNIT. THE SALES REP WILL CONTINUE TO PUSH THE CUSTOMER TOWARDS REPLACING THE INSTRUMENT WITH A IQ. NO FURTHER ACTION REQUIRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22585629 ↗
• MalfunctionFeb 18, 2025Mechanical Problem; Mechanical Problem

  MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF AN AUTOLOG INSTRUMENT, IT WAS REPORTED THAT IT WOULD NOT TRANSFUSE THE BLOOD. THE INSTRUMENT WAS REPLACED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE REPORTED ISSUE DID NOT LEAD TO ADDITIONAL LOSS OF BLOOD. THE PATIENT WAS ALREADY ACTIVELY BLEEDING. THE DEVICE WOULD NOT PROCESS THE BLOOD

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21398539 ↗
• MalfunctionAug 23, 2024Mechanical Problem; Mechanical Problem

  MEDTRONIC RECEIVED INFORMATION THAT AT AN UNSPECIFIED TIME, THIS AUTOLOG INSTRUMENT HAD RBC'S SPILLING INTO THE WASTE BAG. USE OF INSTRUMENT WAS UNSPECIFIED. THERE WAS NO ADVERSE PATIENT EFFECT REPORTED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20050699 ↗