# FDA recall Z-2357-2019

> **Cambridge Sensors Limited** · Class II · device recall initiated 2018-07-26.

## 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.

## Distribution

Illinois

## Key facts

- **Recall number:** Z-2357-2019
- **Recalling firm:** Cambridge Sensors Limited
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-07-26
- **Report date:** 2019-08-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Huntingdon, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2357-2019

## Citation

> AI Analytics. FDA recall Z-2357-2019. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2357-2019. Source: US FDA. Licensed CC0.

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