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FDAFDA · Food and drugs·Recall number Z-1474-2014

Oxoid Legionella Pneumo Groups 2-14, DR0802M, 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.

Published April 30, 2014 · Recall initiated: March 17, 2014

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Remel Inc
Distributor
Distribution was made to CA, FL, IL, MA, ME, NJ, PA, TN, TX, VA, and VT. There was no foreign/military/government distribution.
Lot
DR0802M box lot number 1265362, Exp. 30Jun2014; DR0802 reagent bottle lot number 1265366, exp. June, 2014
Risk classification
Class II
Area (FDA)
device
Country
United States

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