Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
QUIDEL InflammaDry MMP-9 Test Recalled by Quidel Corporation Due to There are two windows on the test device,...
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 Quidel Corporation directly.
Affected Products
QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests
Quantity: 31,140 units
Why Was This Recalled?
There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test results, the positivite test line may not be visible/ hidden under the cassette of the test device thus potentially leading to a false negative result.
Where Was This Sold?
This product was distributed to 44 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MO, MT, NE, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WI, DC
About Quidel Corporation
Quidel Corporation has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report