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Nuvectra recalls

Nuvectra has 2 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 28 Dec 2016. The most frequent reason is lead & heavy metals.

Total recalls2since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 28 Dec 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 2 100%Class III 0 0%

Why nuvectra is recalled

Lead & Heavy Metals2100%

Product types

Spinal Implants2100%

By year

20162100%

All nuvectra recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
28 Dec 2016Device	CLASS II	Algovita Spinal Cord Stimulation System, Percutaneous Leads recalled	Nuvectra	Lead & Heavy Metals	Nationwide
11 May 2016Device	CLASS II	Algovita Spinal Cord Stimulation System Clinical Programmer recalled	Nuvectra	Lead & Heavy Metals	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.