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Caplugs/Evergreen

CAPlugs · Model 500 · UDI-DI 00810044204841

LIB
10
510(k) clearances
8
Adverse events
13
Recalls
54
Facilities

Description

INNOC 10UL LOOP & ARROWHD

Recalls

DateFirmReason
2025-10-23Becton Dickinson & Co.The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an erro
2016-01-08BioMerieux SADiscrepant identification results related to API identification strips. These discrepant identification results are due to false negative results on the tests of the strips linked
2014-10-23Remel IncA reagent within the test may return false negative results.
2014-10-23Remel IncA reagent within the test may return false negative results.
2014-03-17Remel IncA reagent contained within the product may return false negative results.
2014-03-17Remel IncA reagent contained within the product may return false negative results.
2014-03-06BioMerieux SAbioMerieux identified a visual defect and activity issue on the ZYM B reagent (REF 70493) and FB reagent (REF 70562). The activity issue lead to a false negative result of some Ra
2014-03-06BioMerieux SAbioMerieux identified a visual defect and activity issue on the ZYM B reagent (REF 70493) and FB reagent (REF 70562). The activity issue lead to a false negative result of some Ra
2014-03-06BioMerieux SAbioMerieux identified a visual defect and activity issue on the ZYM B reagent (REF 70493) and FB reagent (REF 70562). The activity issue lead to a false negative result of some Ra
2014-03-06BioMerieux SAbioMerieux identified a visual defect and activity issue on the ZYM B reagent (REF 70493) and FB reagent (REF 70562). The activity issue lead to a false negative result of some Ra

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Data 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.