PlainRecalls
FDA Devices Moderate Class II Terminated

Siemens Acute Care pBNP TestPak- in vitro diagnostic test for the quantitative measurement of N-terminal pro-brain natriuretic peptide (NTproBNP) in heparinized plasma. Catalog Number: CPBNPM SMN: 10445086

Reported: January 13, 2016 Initiated: November 11, 2015 #Z-0610-2016

Product Description

Siemens Acute Care pBNP TestPak- in vitro diagnostic test for the quantitative measurement of N-terminal pro-brain natriuretic peptide (NTproBNP) in heparinized plasma. Catalog Number: CPBNPM SMN: 10445086

Reason for Recall

Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

Details

Units Affected
1157
Distribution
Worldwide Distribution - US (nationwide), Algeria, Armenia, Australia, Austria, Bangladesh, Bosnia Herzegovina, Canada, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Ireland, Italy, Japan, Libya, Malaysia, Poland, Portugal, Romania, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, U.A.E., and United Kingdom.
Location
Norwood, MA

Frequently Asked Questions

What product was recalled?
Siemens Acute Care pBNP TestPak- in vitro diagnostic test for the quantitative measurement of N-terminal pro-brain natriuretic peptide (NTproBNP) in heparinized plasma. Catalog Number: CPBNPM SMN: 10445086. Recalled by Siemens Healthcare Diagnostics Inc. Units affected: 1157.
Why was this product recalled?
Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Which agency issued this recall?
This recall was issued by the FDA Devices on January 13, 2016. Severity: Moderate. Recall number: Z-0610-2016.