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

Recall Z-1473-2014 — Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.

U.S. FDA — Device Enforcement · United States · 2014-03-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1473-2014
Date of alert: 2014-03-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Remel Inc
Product category: device
Product type: Devices

Reported risk: A reagent contained within the product may return false negative results.

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.

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.

Recall Z-1473-2014 — Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.

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