Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within the test may return false...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Remel Inc directly.
Affected Products
Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Latex Reagent, DR0802, Lot 1301912. The responsible firm on the label is Oxoid Ltd.
Quantity: 59/50 test boxes
Why Was This Recalled?
A reagent within the test may return false negative results.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Remel Inc
Remel Inc has 70 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report