FDA recall Z-0553-2018

The Binding Site Group, Ltd. · Class II · device

Product

Rheumatoid Factor (RF) Kit for use on SPAPLUS, Product #LK151.S.A Intended for the quantitative in-vitro measurement of rheumatoid factor in serum using the Binding Site SPAPLUS analyser. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis. This test should be used in conjunction with other laboratory and clinical findings

Reason for recall

The low and high controls for the product are returning results above the assigned values.

Distribution

US Distribution was made to CA. There was no foreign/military/government distribution.

Key facts

Status
Terminated
Initiation date
2018-01-04
Report date
2018-02-14
Termination date
2020-06-09
Voluntary/Mandated
Voluntary: Firm initiated
Location
Birmingham, N/A, United Kingdom

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0553-2018