Z-0697-2016 Class II Terminated

Recalled by Phadia Ab — Uppsala, N/A

Recall Details

Product Type
Devices
Report Date
February 3, 2016
Initiation Date
December 28, 2015
Termination Date
August 16, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
76

Product Description

EliA SmDP Well, Article Number 14-5624-01 Product Usage: EliA SmDP is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to Sm in human serum and plasma (EDTA, citrate) as an aid in the clinical diagnosis of systemic lupus erythematosus (SLE) in conjunction with other laboratory and clinical findings. EliA SmDP uses the EliA IgG method on the instruments Phadia 100 and Phadia 250.

Reason for Recall

All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA SmDP well lot 0018 may be incorrect and must be considered invalid. Patient samples in complaint investigations caused unspecific signals up to 22 U/ml on EliA SmDP well lot 0018. The nonspecific signals are not caused by anti-Sm antibodies, nor by streptavidin antibodies.

Distribution Pattern

US Nationwide in the states of NC, GA, NJ, NY, PA, TX, IL, MI, MT, NM, and OR.

Code Information

Product number: 14-5624-01 Lot: 0018 Exp date: 11/30/2016