Abbott Laboratories Inc. (St Jude Medical) recalls

Abbott Laboratories Inc. (St Jude Medical) has 5 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 23 Jun 2021. The most frequent reason is device malfunction.

Total recalls5since 2019

Last 12 months0reported

Class I00% of total

Ongoing0latest 23 Jun 2021

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 5 100%Class III 0 0%

Why abbott laboratories inc. (st jude medical) is recalled

Device Malfunction5100%

Product types

By year

2021480%
2019120%

All abbott laboratories inc. (st jude medical) recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
23 Jun 2021Device	CLASS II	v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate recalled	Abbott Laboratories Inc. (St Jude Medical)	Device Malfunction	Nationwide
23 Jun 2021Device	CLASS II	WorkMate Claris v.1.2 Upgrade Kits recalled	Abbott Laboratories Inc. (St Jude Medical)	Device Malfunction	Nationwide
23 Jun 2021Device	CLASS II	v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate recalled	Abbott Laboratories Inc. (St Jude Medical)	Device Malfunction	Nationwide
19 May 2021Device	CLASS II	NeuroTherm NT2000iX Radiofrequency (RF) Generator recalled	Abbott Laboratories Inc. (St Jude Medical)	Device Malfunction	MN
5 Jun 2019Device	CLASS II	TactiSys Quartz Equipment (with recalled by Abbott Laboratories Inc. (St	Abbott Laboratories Inc. (St Jude Medical)	Device Malfunction	MN

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.