LumiQuick PCP Test Strips Recalled for Unapproved Distribution
LumiQuick Diagnostics Inc. is recalling PCP Test Strips distributed to US locations without approved PMA, IDE, or 510(k) clearance.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity score. The hazard is regulatory (unapproved distribution) rather than a direct physical injury or high-risk pathogen, and no illnesses or injuries are reported in the source text.
Plain-English summary
LumiQuick Diagnostics Inc. is recalling PCP Test (Strip) products, catalog number 74033, all lots. The recall is due to the distribution of these products to US locations that do not have approved applications for Premarket Approval (PMA), Investigational Device Exemption (IDE), or 510(k) clearance.
The affected products were distributed in the states of California, Florida, New Jersey, Texas, and New York. The recall covers all lots of the PCP Test (Strip) manufactured by LumiQuick Diagnostics Inc. in Santa Clara, CA.
Consumers and healthcare providers who have received these products should stop using them and contact the recalling firm for further instructions.
The recalled product
- Product
- PCP Test (Strip); LumiQuick, Santa Clara, CA 95054
- Manufacturer
- LumiQuick Diagnostics Inc.
- Category
- Medical Device — Diagnostic Test
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Catalog number: 74033
- All lots
Distribution
Part of a larger recall action
This product is one of 80 recalled by LumiQuick Diagnostics Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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