Abbott Laboratories Inc. (St Jude Medical) recalls
Every recall we track for Abbott Laboratories Inc. (St Jude Medical) — 5 in all, from 2019–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Abbott Laboratories Inc. (St Jude Medical) peaked in 2021 (4); 5 since 2017.
All FDA recall records for Abbott Laboratories Inc. (St Jude Medical) since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 4 | 0 | 4 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Abbott Laboratories Inc. (St Jude Medical) product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Abbott Laboratories Inc. (St Jude Medical) recalls
3 shown- Lower riskMedical device
Abbott Laboratories Inc. (St Jude Medical) recalls v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System Display, Model H700124, The WorkMate Claris"
St Jude Medical recalls WorkMate Claris System Display Model H700124 with v.1.2 software upgrade that may cause screen blackouts during use. Affected units include specific serial numbers listed in the recall.
St Jude MedicalMay 5, 2021 - Lower riskMedical device
Abbott Laboratories Inc. (St Jude Medical) recalls NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000
St Jude Medical recalls NeuroTherm NT2000iX Radiofrequency Generators with serial numbers listed. Potential capacitor failure may cause output issues or charring/smoky odor. Consumers should check if their device has listed serial numbers.
St Jude MedicalApr 22, 2021 - Lower riskMedical device
Abbott Laboratories Inc. (St Jude Medical) recalls TactiSys Quartz Equipment (with software version 1.7) Model: PN-004 400 Part Numbers: 600043767 (China), 100154367
St Jude Medical recalls TactiSys Quartz Equipment with software version 1.7.0 due to potential log data storage issues. Affected units may display incorrect contact force data during procedures.
St Jude MedicalApr 5, 2019
Abbott Laboratories Inc. (St Jude Medical) recall questions
How many recalls has Abbott Laboratories Inc. (St Jude Medical) had?
5 recalls from Abbott Laboratories Inc. (St Jude Medical) are on record with U.S. safety agencies, from 2019–2021.
What is the most recent Abbott Laboratories Inc. (St Jude Medical) recall?
Abbott Laboratories Inc. (St Jude Medical) recalls v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System Display, Model H700124, The WorkMate Claris", dated May 5, 2021. Every Abbott Laboratories Inc. (St Jude Medical) recall is listed on this page, newest first.
What should I do if I have a recalled Abbott Laboratories Inc. (St Jude Medical) product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Abbott Laboratories Inc. (St Jude Medical) recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.