Official recall record
QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-03-05
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 30014613336747
- Brand on record
- Quidel Corporation
- Product category
- Medical Device
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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