ImmunoFLOW Negative Control Mycoplasma IgM
GenBio · Model 800-3921 · UDI-DI 00613745000145
LJZ
Prescription
10
510(k) clearances
0
Adverse events
4
Recalls
14
Facilities
Description
Mycoplasma IgM Negative Control contains human serum without reactivity to Mycoplasma pneumoniae complement–fixing antigen and is used in conjunction with the appropriate ImmunoFLOW Assay Test System.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-02-08 | Meridian Bioscience Inc | Use of the kits after incorrect storage could lead to a potential false-negative or invalid result. In the event of a false-negative, the incorrect assumption would be made as to t |
| 2008-08-27 | Calbiotech Inc | The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, |
| 2008-08-27 | Calbiotech Inc | The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, |
| 2008-08-27 | Calbiotech Inc | The recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall, |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
