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QiG Group recalls

QiG Group has 3 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 30 Mar 2016. The most frequent reason is device malfunction.

Total recalls3since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 30 Mar 2016

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 3 100%Class III 0 0%

Why qig group is recalled

Device Malfunction3100%

Product types

Other Medical Devices3100%

By year

20163100%

All qig group recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
30 Mar 2016Device	CLASS II	Algostim LLC, Algovita Implanted Pulse Generator stimulator recalled	QiG Group	Device Malfunction	MN
30 Mar 2016Device	CLASS II	Algostim LLC, Algovita External Pulse Generator, Trial Stimulator recalled	QiG Group	Device Malfunction	MN
30 Mar 2016Device	CLASS II	Algostim LLC, Algovita Implanted Pulse Generator stimulator recalled	QiG Group	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.