Abiomed, Inc. recalls Automated Impella Controller (AIC)
Reason for recall
Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC).
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 4. Impella Controller, Packaged, EU, Loaner; Product Code: 0042-0000-EU-L. 5. Impella Controller, Packaged, IN; Product Code: 0042-0000-IN. 6. Impella Controller, Packaged, JP; Product Code: 0042-0000-JP. 7. Impella Controller, Japan, Loaner; Product Code: 0042-0000-JP-L. 8. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK. 9. Impella Controller, UK, Loaner; Product Code: 0042-0000-UK-L. 10. Impella Controller, Packaged, US; Product Code: 0042-0000-US. 11. Impella Controller, Packaged, US, Loaner; Product Code: 0042-0000-US-L. 12. Impella Optical Controller, Packaged, AU; Product Code: 0042-0010-AU. 13. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU. 14. Impella Optical Controller, EU, Loaner; Product Code: 0042-0010-EU-L. 15. Impella Optical Controller, Packaged, IN; Product Code: 0042-0010-IN. 16. Impella Optical Controller, Packaged, UK; Product Code: 0042-0010-UK. 17. Impella Optical Controller, UK, Loaner; Product Code: 0042-0010-UK-L. 18. Impella Optical Controller, Packaged, US; Product Code: 0042-0010-US. 19. Impella Optical Controller, US, Loaner; Product Code: 0042-0010-US-L. 20. Optical, AIC, Impella Connect, Pkgd, AU; Product Code: 0042-0040-AU. 21. Optical AIC w/Impella Connect,Pack'd, CA; Product Code: 0042-0040-CA. 22. AIC w/Remote Link, Pkgd, Cln Trl, US; Product Code: 0042-0040-CT. 23. AIC w/Remote Link, Pkgd, Cln Trl, US; Product Code: 0042-0040-CT-L. 24. Optical AIC w/Impella Connect,Pack'd, EU; Product Code: 0042-0040-EU. 25. Optical AIC w/Impella Connect,EU,Loaner; Product Code: 0042-0040-EU-L. 26. Optical AIC w/Impella Connect, Pkgd, JP; Product Code: 0042-0040-JP. 27. Optical AIC w/Impella Connect, Pkgd, JP; Product Code: 0042-0040-JP-L. 28. Optical, AIC, Impella Connect, Pkgd, UK; Product Code: 0042-0040-UK. 29. Optical, AIC, Impella Connect, Pkgd, US; Product Code: 0042-0040-US. 30. Optical AIC Impella Connect, US, Loaner; Product Code: 0042-0040-US-L. 31. Dbl optical, AIC Impella Connect, Phg US; Product Code: 1000201. 32. AIC w/Impella Connect for ECP; Product Code: 1000432.
Lot / code information
- GTIN
- 813502010886; All
- Serial #
- . 2. Product Code: 0042-0000-CA
- GTIN
- 813502011272; All
- Serial #
- . 3. Product Code: 0042-0000-EU
- GTIN
- 813502011289; All
- Serial #
- . 4. Product Code: 0042-0000-EU-L
- GTIN
- 813502011289; All
- Serial #
- . 5. Product Code: 0042-0000-IN
- GTIN
- 813502011418; All
- Serial #
- . 6. Product Code: 0042-0000-JP
- GTIN
- 813502010428; All
- Serial #
- . 7. Product Code: 0042-0000-JP-L
- GTIN
- 813502010428; All
- Serial #
- . 8. Product Code: 0042-0000-UK
- GTIN
- 813502011296; All
- Serial #
- . 9. Product Code: 0042-0000-UK-L
- GTIN
- 813502011296; All
- Serial #
- . 10. Product Code: 0042-0000-US
- GTIN
- 813502010022; All
- Serial #
- . 11. Product Code: 0042-0000-US-L
- GTIN
- 813502010022; All
- Serial #
- . 12. Product Code: 0042-0010-AU
- GTIN
- 813502010930; All
- Serial #
- . 13. Product Code: 0042-0010-EU
- GTIN
- 813502010961; All
- Serial #
- . 14. Product Code: 0042-0010-EU-L
- GTIN
- 813502010961; All
- Serial #
- . 15. Product Code: 0042-0010-IN
- GTIN
- 813502011425; All
- Serial #
- . 16. Product Code: 0042-0010-UK
- GTIN
- 813502010978; All
- Serial #
- . 17. Product Code: 0042-0010-UK-L
- GTIN
- 813502010978; All
- Serial #
- . 18. Product Code: 0042-0010-US
- GTIN
- 813502010985; All
- Serial #
- . 19. Product Code: 0042-0010-US-L
- GTIN
- 813502010985; All
- Serial #
- . 20. Product Code: 0042-0040-AU
- GTIN
- 813502012972; All
- Serial #
- . 21. Product Code: 0042-0040-CA
- GTIN
- 813502012958; All
- Serial #
- . 22. Product Code: 0042-0040-CT
- GTIN
- 813502011722; All
- Serial #
- . 23. Product Code: 0042-0040-CT-L
- GTIN
- 813502011722; All
- Serial #
- . 24. Product Code: 0042-0040-EU
- GTIN
- 813502012217; All
- Serial #
- . 25. Product Code: 0042-0040-EU-L
- GTIN
- 813502012217; All
- Serial #
- . 26. Product Code: 0042-0040-JP
- GTIN
- 813502011814; All
- Serial #
- . 27. Product Code: 0042-0040-JP-L
- GTIN
- 813502011814; All
- Serial #
- . 28. Product Code: 0042-0040-UK
- GTIN
- 813502012484; All
- Serial #
- . 29. Product Code: 0042-0040-US
- GTIN
- 813502011401; All
- Serial #
- . 30. Product Code: 0042-0040-US-L
- GTIN
- 813502011401; All
- Serial #
- . 31. Product Code: 1000201
- GTIN
- 813502010442; All
- Serial #
- . 32. Product Code: 1000432
- GTIN
- 813502013030; All
Show 53 more code fieldsShow fewer
What the firm is doing
Abiomed notified consignees via UPS delivery on about 10/01/2025. Consignees were informed of the potential cybersecurity vulnerabilities related to network and physical access. Next steps included that product was not being removed, to maintain the affected device in a secure environment with restricted access, and an Abiomed field representative will contact consignees to arrange disabling the AIC's network capabilities. Consignees were instructed to review the notice and forward it to applicable personnel or customers if further distributed, report any suspicions of a cybersecurity event, and complete and return the response form. A follow up notification was sent to non-responding consignees on about 11/12/2025. The letter informed consignees that they were being contacted because they have not returned the response to the first notification. If a completed Business Reply Form is not received before a third notification letter (approximately 30 days), Abiomed will proactively disable remote viewing capabilities on Impella Connect.
DistributionShow detailsHide
Nationwide distribution. International distribution to United Arab Emirates, Austria, Australia, Belgium, Brunei Darussalam, Brazil, Canada, Switzerland, Colombia, Czechia, Germany, Denmark, Spain, Finland, France, United Kingdom of Great Britain and Northern Ireland, Greece, Hong Kong, Croatia, Ireland, Israel, India, Italy, Japan, Kuwait, Luxembourg, Mexico, Malaysia, Netherlands, Norway, New Zealand, Panama, Pakistan, Poland, Serbia, Saudi Arabia, Sweden, Singapore, Slovenia, Thailand, Taiwan.
A reasonable probability that use of the product will cause serious adverse health consequences or death.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-0069-2026
- FDA device classification · OZDOfficial FDA classification for this device type
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Abiomed, Inc.Search for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
More Class I recalls
Medtronic Heart Valves Division recalls Medtronic Harmony Delivery Catheter System
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a man…
- Pulmonary Valve Prosthesis Percutaneously Delivered
- Process control
Windstone Medical Packaging, Inc. recalls A M S
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
- General Surgery Tray
- Material/Component Contamination
Windstone Medical Packaging, Inc. recalls A M S
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
- General Surgery Tray
- Material/Component Contamination
