TB4 Glu/Lac Test/Blank Sensor
Blank Sensor used For GLU or LAC on Siemens Healthcare Diagnostics RAPIDLab® Series systems.
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
7recalls on this code
Who Else Makes It
Concentrated in Shandong (1), Hunan (1), Jiangsu (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Biobase Biodustry(Shandong)Co., Ltd. | Jinan | Shandong | Manufacturer | 70 |
| AVE Science & Technology Co., Ltd. | Changsha | Hunan | Manufacturer | 22 |
| Eaglenos Sciences, Inc. | Nanjing | Jiangsu | Manufacturer | 4 |
Record
| Listed by | Siemens Healthcare Diagnostics Inc, United States |
|---|---|
| FDA product code | KHP |
| Device type | Acid, Lactic, Enzymatic Method |
| Device class | Class 1 |
| Regulation | 21 CFR 862.1450 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K031560 |
| Record published | 2016-09-24 |
| Record revised | 2021-11-19 (version 6) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | lot or batch number, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 10326708 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| StatSensor/StatStrip | Nova Biomedical Corporation | 5 |
| Stat Profile | Nova Biomedical Corporation | 5 |
| Lactate Gen.2 | Roche Diagnostics Gmbh | 4 |
| Lactate Plus | Nova Biomedical Corporation | 4 |
| Biobase | Biobase Biodustry(Shandong)Co., Ltd. | 3 |
| i-STAT | Abbott Point OF Care Inc. | 3 |
| Alinity | Abbott Medical | 2 |
| Fora | Fora Care Inc. | 2 |
| Vitros | Ortho-Clinical Diagnostics, Inc. | 2 |
| LA Cartridge | LifeHealth, LLC | 2 |
| L-Lactate (LAC) | Randox Laboratories Limited | 2 |
| ABX Pentra Lactic Acid | Horiba ABX SAS | 1 |
Showing 12 of 43. All products under Acid, Lactic, Enzymatic Method
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K113216 | 2012-05-03 |
Recalls Naming This Product
14 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2018-07-16 | Class II | Device Design | Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere with tHb and some of the CO-Ox fractions that are reported on the RAPIDPoint and RAPIDLab Blood Gas systems indicated. This may cause lower than expected values for ca | 138 | 2020-06-23 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2018-07-16 | Class II | Device Design | Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere with tHb and some of the CO-Ox fractions that are reported on the RAPIDPoint and RAPIDLab Blood Gas systems indicated. This may cause lower than expected values for ca | 2357 | 2020-06-23 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2017-04-10 | Class II | Software design | Potential Patient Demographic Error with Blank Patient ID Field | 159 units | 2019-08-20 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2016-08-11 | Class II | Software design | There is a potential for the first and/or last name of one patient to be printed with Patient ID and result data from a different patient, even though those fields have been turned Off for the system | 144 units | 2020-07-16 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2016-08-11 | Class II | Software design | There is a potential for the first and/or last name of one patient to be printed with Patient ID and result data from a different patient, even though those fields have been turned Off for the system | 197 units | 2020-07-16 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2015-05-06 | Class II | Software design | D50 and D51 Diagnostic error codes are not functional. | 122 devices | 2017-08-02 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2012-09-17 | Class II | Software Manufacturing/Software Deployment | RAPIDPoint 400 Series, RAPIDPoint 500, or RAPIDLab 1200 Series blood gas analyzer, users can inadvertently enter a wrong patient ID on the demographics screen, which ultimately could lead to a misidentification of the sample | 179 units | 2015-04-01 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2012-09-17 | Class II | Software Manufacturing/Software Deployment | RAPIDPoint 400 Series, RAPIDPoint 500, or RAPIDLab 1200 Series blood gas analyzer, users can inadvertently enter a wrong patient ID on the demographics screen, which ultimately could lead to a misidentification of the sample | 274 units | 2015-04-01 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2006-04-04 | Not classified | Software design | Invalid CO-oximeter values; Bayer HealthCare determined that under very specific conditions, the RapidLab 1245 or RapidLab 1265 systems may report invalid CO-oximeter values to an LIS, Rapidlink, or Rapidcomm data management system. | Domestic – 124 units, Foreign-364 units (all systems) | 2012-07-30 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2006-04-04 | Not classified | Software design | Invalid CO-oximeter values; Bayer HealthCare determined that under very specific conditions, the RapidLab 1245 or RapidLab 1265 systems may report invalid CO-oximeter values to an LIS, Rapidlink, or Rapidcomm data management system. | Domestic – 124 units, Foreign-364 units (all systems) | 2012-07-30 |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2006-01-20 | Not classified | Other | When stored data is recalled from memory, the results do not agree with the original results. Software anomaly: a calculation error occurs when using the correlation adjustment feature on the RapidLab 1200 Systems with software versions 1. | 2012-05-02 | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2006-01-20 | Not classified | Other | When stored data is recalled from memory, the results do not agree with the original results. Software anomaly: a calculation error occurs when using the correlation adjustment feature on the RapidLab 1200 Systems with software versions 1. | 2012-05-02 | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2006-01-20 | Not classified | Other | When stored data is recalled from memory, the results do not agree with the original results. Software anomaly: a calculation error occurs when using the correlation adjustment feature on the RapidLab 1200 Systems with software versions 1. | 2012-05-02 | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2006-01-20 | Not classified | Other | When stored data is recalled from memory, the results do not agree with the original results. Software anomaly: a calculation error occurs when using the correlation adjustment feature on the RapidLab 1200 Systems with software versions 1. | 2012-05-02 |
Recalls
6 of these are Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-07-05 | Class III | Under Investigation by firm | Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved for shipment in the United States | 76 | 2017-08-02 |
| 2015-08-24 | Class II | Process control | RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through 2519000012, negative sodium bias on both QC and patient results | 2079 cartridges | 2016-05-23 |
| 2015-08-24 | Class II | Process control | RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through 2519000012, negative sodium bias on both QC and patient results | 49 cartridges | 2016-05-23 |
| 2015-08-24 | Class II | Process control | RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through 2519000012, negative sodium bias on both QC and patient results | 982 cartridges | 2016-05-23 |
| 2015-08-24 | Class II | Process control | RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through 2519000012, negative sodium bias on both QC and patient results | 1213 cartridges | 2016-05-23 |
| 2015-07-28 | Class II | Software design | When both ports (Serial and Ethernet) are configured to transmit data, the data stream from one port could potentially affect the data stream from the other port causing the data management system to include either: duplicate data, missing | 5241 units | 2017-02-17 |
| 2014-05-23 | Class II | Process design | RAPIDPoint 500 Measurement Cartridges may have an error code one or more electrolyte parameters (e.g., Na+, Ca++, K+, Cl-) | 20,507 cartridges | 2015-06-10 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.