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

Recall Z-2350-2015 — PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. Latex agglutination test for identification of beta-hemolytic streptococci of Lancefield Groups A, B, C, F or G from primary culture plates.

U.S. FDA — Device Enforcement · United States · 2015-06-30 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2350-2015
Date of alert
2015-06-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Remel Inc
Product category
device
Product type
Devices
Reported risk: A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

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.