Microdot Xtra blood glucose test strips — Class II medical device recall Z-2357-2019
Ongoing recall by Cambridge Sensors Limited, reported 2019-08-28, distributed in IL. The firm reported that a faulty cutting/punching machine did not meet specifications after being fitted with n
| Recall number | Z-2357-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cambridge Sensors Limited, Huntingdon, N/A, United Kingdom |
| Recall initiated | 2018-07-26 |
| Classified | 2019-08-22 |
| Reported by FDA | 2019-08-28 |
| Distributed | IL |
| Quantity | 17,784 |
| Lot numbers | 7091101, 7091201, 7091801, 7091902, 7100402, 7100403, 7101002, 7101602, 7101702, 7102403, 7103002, 7110602, 7110703, 7112702 |
Product
Microdot Xtra blood glucose test strips
Reason for recall
The firm reported that a faulty cutting/punching machine did not meet specifications after being fitted with new blades and did not correctly "notch" BG test strips intended for use in the US. The impacted strips did not fit into the inlet port of the BG meter, therefore resulting in a delay in BG testing and results.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2357-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.