BIO-RAD LABORATORIES INC
D-10 · Cardiovascular
510(k) Clearances (4)
Substantially Equivalent
Substantially Equivalent
Substantially Equivalent
Substantially Equivalent
Recalls (9)
On a rare occasion, there is a potential to assign a patient result to an incorrect sample ID when running in D10 Rack Loader configuration.
On a rare occasion the D-10 software might generate an extra result by duplicating the result form the previous sample and the Sample ID/Injection number from the next sample.
D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge injections counts are not being updated correctly when switching between the D-10 Dual Short Program and Extended Program on the D-10 Hemoglobin Testing System.
A previous recall related to reports of calibration failure and late retention times using Elution Buffer led to an examination of other buffers manufactured during the same time period and a decision was made to field correct these products until a definitive root cause and corrective action have been found and implemented.
A previous recall related to reports of calibration failure and late retention times using Elution Buffer led to an examination of other buffers manufactured during the same time period and a decision was made to field correct these products until a definitive root cause and corrective action have been found and implemented.
A previous recall related to reports of calibration failure and late retention times using Elution Buffer led to an examination of other buffers manufactured during the same time period and a decision was made to field correct these products until a definitive root cause and corrective action have been found and implemented.
Reports of calibration failure and late retention time using Elution Buffer AA10434 and AA10435.
The firm discovered that the Update Kit Floppy Diskette included in the reorder pack was mislabeled with an incorrect Lot Number for the Calibrator/Diluent Set as: S01819; The correct Lot Number for the Calibrator/Diluent Set is: S01704.
The Diluent in the D-10 Dual Program Calibrator reorder packs is defective, and can cause early calibration failure or elevated control and sample recovery results.
UDI Registrations (20)
D-10 Wash/Diluent Solution
D-10 Hemoglobin A1c Program Calibrator/Diluent Set
D-10 Sample Vials
D-10 Hemoglobin A1c Program
D-10 Hemoglobin A1c Program Analytical Cartridge
D-10 Analytical Cartridge Hemoglobin A1c Program or Hemoglobin A2/F/A1c Program
D-10 Hemoglobin Testing System
D-10 Dual Program Reorder Pack
D-10 Dual Program HbA2/F/A1c Calibrator/Diluent Set
D-10 Hemoglobin Testing System
D-10 Analytical Cartridge Hemoglobin A1c Program
D-10 Hemoglobin A1c Program Elution Buffer 1
D-10 Hemoglobin A1c Program Elution Buffer 2
D-10 Dual Program HbA1c Calibrator/Diluent Set
D-10 Dual Program Elution Buffer 2
D-10 Hemoglobin A1c Supplemental Reagent Pack
D-10 Hemoglobin A1c Program REORDER PACK
D-10 Hemoglobin A1c Program Calibrator/Diluent Set
D-10 Dual Program Elution Buffer 1
MAUDE Adverse Events (1)
FDA Classification (63)
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular
Cardiovascular