Euro Diagnostica AB

8 recalls β€’ β€’ Categories: Diagnostic Equipment, Infusion Pumps

Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.

Oct 21, 2016 Diagnostic Equipment View Details β†’

Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.

Oct 21, 2016 Infusion Pumps View Details β†’

Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.

Oct 21, 2016 Diagnostic Equipment View Details β†’

Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.

Oct 21, 2016 Infusion Pumps View Details β†’

Complaint investigation concluded that although product quality requirements stated in the instructions for use were met at lot release, the high background in the ELISA plate, the strong IgM conjugate, and the low reference control led to an increased risk of equivocal and/or false positive sample test results for the two FANA200 kit lots SS 1500 and SS 2009.

Oct 15, 2015 Diagnostic Equipment Nationwide View Details β†’

Euro Diagnostica has identified a deviation in one of the components of the DIASTAT ANA (FANA200), lot TS 2076. The kit might not perform correctly and so potentially yield false positive samples.

Feb 14, 2017 Diagnostic Equipment View Details β†’

FANA200 kit lot TS 3577 was re-worked due to shortened shelf-life. The alert sticker on the kit box of the lot informed customers that the shelf-life had been shortened and referenced a letter sent to customers for more information, where the new expiration date was stated. The original kit box label remained on the kit box stating the original expiration date, the packaging did not display the correct expiration date.

May 22, 2017 Diagnostic Equipment View Details β†’