Class II — Cambridge Sensors Limited
| Recalling firm | CAMBRIDGE SENSORS LIMITED |
|---|---|
| Registered facility | CAMBRIDGE SENSORS LIMITED (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | 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. |
| Product | Microdot Xtra blood glucose test strips |
| Quantity | 17,784 (USA) |
| Distribution | Illinois |
| Initiated | 2018-07-26 |
| Classified | 2019-08-22 |
| Recall number | Z-2357-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Cambridge Sensors Limited (Z-2357-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82867/
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