HYTEC 288 System, Model 74007P, automated immunoanalyzer (EIA) instrument. For in vitro diagnostic use only. HYTEC AUTOSTAT II RF assays: HYTEC AUTOSTAT II RF IgM Kit: Part Number FGA 05, HYTEC AUTOSTAT II RF IgA Kit: Part Number FGA 06, HYTEC AUTOSTAT II RF IgG Kit: Part Number FGA 07, HYTEC AUTOSTAT II Total Rheumatoid Factor Kit: Part Number FGA 08.
Recall
- Recall Number
- Z-2200-2019
- Event Number
- 83268
- Firm
- Hycor Biomedical Inc
- FEI Number
- 1000125787
- Product Code
- DHR
- Status
- Open, Classified
- Root Cause
- Labeling design
- Initiated
- March 19, 2018
- Address
- 7272 Chapman Ave, Garden Grove, CA, 92841-2103
Description
HYTEC 288 System, Model 74007P, automated immunoanalyzer (EIA) instrument. For in vitro diagnostic use only. HYTEC AUTOSTAT II RF assays: HYTEC AUTOSTAT II RF IgM Kit: Part Number FGA 05, HYTEC AUTOSTAT II RF IgA Kit: Part Number FGA 06, HYTEC AUTOSTAT II RF IgG Kit: Part Number FGA 07, HYTEC AUTOSTAT II Total Rheumatoid Factor Kit: Part Number FGA 08.
Reports when using Rheumatoid Factor test kits, control and negative samples may be elevated following a sample containing high levels of IgG . The negative control may report out of range; a negative sample may recover as a low positive which could contribute to an incorrect or premature diagnosis of rheumatoid.
On March 19, 2018, Hycor Biomedical sent a "Urgent Field Safety Notice" via Federal Express to consignees. The urgent field safety notices recommending the following steps to detect and minimize possible sample carryover: 1. Repeat testing of all patient samples for the HYTEC AUTOSTAT II RF assays when the negative control reports out of range. 2. Do not perform HYTEC AUTOSTAT II RF assays in batch mode. HYTEC AUTOSTAT II RF should be tested independently of all other autoimmune assays. 3. Performing testing in duplicate may assist in detecting potential carryover of high levels of IgG from one sample into another reaction well. If the duplicate results do not match, sample carryover may be the root cause. 4. The needle tip of the single tip arm should be cleaned weekly, according to the recommended maintenance schedule. The needle tip should be inspected for damage; a damaged needle tip should be replaced by trained service personnel. 5. It is mandatory that all consignees complete and return the enclosed response within 10 days of receipt, in order for us to verify your understanding of this Field Safety Notice. If you have any questions, please contact Hycor Biomedical at 714-933-3000
Worldwide distribution to US state of TX , Netherlands, Belgium, Austria, Italy, and India
288