autoLog® ATLG110 (UDI 00673978521916)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00673978521916), received between Apr 3, 2023 and Jul 23, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (2 reports).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 23, 2024Mechanical Problem; Mechanical Problem

  MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF AN AUTOLOG IQ INSTRUMENT, IT WAS REPORTED THAT THE AMOUNT OF BLOOD CELLS THE CUSTOMER WAS GETTING BACK WAS LESS THAN THEY ARE USED TO. THE INSTRUMENT WAS REPLACED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19805188 ↗
• MalfunctionApr 3, 2023Device Alarm System; Mechanical Problem; Device Alarm System; Mechanical Problem

  MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF AN AUTOLOG INSTRUMENT, IT WAS REPORTED THAT THE INSTRUMENT WOULD NOT PUMP BLOOD TO THE HOLDING BAG AND IT GAVE A ROLLER PUMP ERROR. IT WAS STATED THAT THE INSTRUMENT'S CENTRIFUGE MADE A RATTLING SOUND. 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 DAMAGE TO INSTRUMENT. THE CUSTOMER REPLACED THE ENTIRE DEVICE AND KIT. THE BLOOD THAT WAS NOT SENT TO THE HOLDING BAG WAS DISCARDED. THE BLOOD WAS NOT PROCESSED IN THE IN BACKUP INSTRUMENT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE PATIENT DID NOT RECEIVE A TRANSFUSION OF NON-AUTOLOGOUS BLOOD BECAUSE OF THIS ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16661903 ↗

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 · Terminated
  Hospital 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