InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit - 10 pack. Model Number: 90010.
FDA device recall Z-0725-2026 · posted 2025-11-28 · Open, Classified
Recall details
- Recalling firm
- Enterix, Inc.
- Reason for recall
- InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.
- Action taken
- Consignees were initially sent an email as notification of the recall on about 09/17/2025, which was followed by a formal recall notification letter on about 09/23/2025. Consignees were instructed to immediately examine inventory and quarantine any affected units, notify customers if affected further distributed, and for those patients that have already been tested using an InSure ONE test kit that has been identified as part of the scope of this recall be retested. Once an inventory count has been received by Enterix, they will provide RMA and courier information so the recalled product can be returned for sorting and destruction.
- Root cause
- Under Investigation by firm
- Status
- Open, Classified
- Product code
- KHE
- Quantity affected
- 201,426 test kits
- Distribution
- Worldwide - US Nationwide distribution in the states of California, Florida, Georgia, Illinois, Indiana, Kentucky, Massachusetts, Nevada, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Texa
- Date initiated
- 2025-09-17
- Date posted
- 2025-11-28
- Location
- Edison, NJ
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| InSure ONE (K170548) | Enterix, Inc. | 2017-10-05 |