Phadia Ab recalls

Phadia Ab has 5 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 31 Jan 2024. 1 is still ongoing.

Total recalls5since 2016

Last 12 months0reported

Class I00% of total

Ongoing1latest 31 Jan 2024

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 phadia ab is recalled

Product types

Test Kits & Diagnostics5100%

By year

2024120%
2019240%
2018120%
2016120%

Ongoing phadia ab recalls

1 active

Reported	Class	Recall	Company	Reason	Where
31 Jan 2024Device	CLASS II	EliA GBM Wells, Material Number 14551401, for Phadia recalled	Phadia Ab	Other	Nationwide

All phadia ab recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
31 Jan 2024Device	CLASS II	EliA GBM Wells, Material Number 14551401, for Phadia recalled	Phadia Ab	Other	Nationwide
4 Sep 2019Device	CLASS II	Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is recalled	Phadia Ab	Device Malfunction	Nationwide
10 Jul 2019Device	CLASS II	EliA RF IgM Well recalled by Phadia Ab	Phadia Ab	Potency & Assay	Nationwide
11 Apr 2018Device	CLASS II	Phadia Prime recalled by Phadia Ab	Phadia Ab	Potency & Assay	13 states
3 Feb 2016Device	CLASS II	EliA SmDP Well, Article Number recalled by Phadia Ab	Phadia Ab	Other	Nationwide

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.