Product Wiki · Recalls · U.S. FDA — Device Enforcement

API Listeria (REF 10300). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the APIs are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms. — recall Z-1478-2014

U.S. FDA — Device Enforcement · France · 2014-03-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1478-2014
Date of alert
2014-03-06
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
BioMerieux SA
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
1002569040
Reported risk: bioMerieux 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 Rapid ID 32 strips and API biochemical tests using the ZYM B reagent or FB reagent
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.