Brand

Phadia Ab Recalls

4 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Phadia Ab.

4Total Recalls
0Critical
127,341Units Affected
May 24, 2023Most Recent
All Recalls

Every Phadia Ab Recall

Sorted by most recent. Click any recall for full details.

4 recalls
High RiskFDA
Phadia Ab
EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000. In vitro diagnostic
Diagnostic Devices·124,928 affected·May 24, 2023
High RiskFDA
Phadia Ab
EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measurement of IgM clas...
Medical Devices·30 affected·May 10, 2019
High RiskFDA
Phadia Ab
Phadia Prime software, article number 12-4101-00, as used in combination with the Phadia 250 Instrument, article number 12-3900-01 and El...
Diagnostic Devices·2,307 affected·Nov 20, 2017
High RiskFDA
Phadia Ab
EliA SmDP Well, Article Number 14-5624-01 Product Usage: EliA SmDP is intended for the in vitro semi-quantitative measurement of IgG ...
Medical Devices·76 affected·Dec 28, 2015