FDAJuly 26, 2018device
Microdot Xtra blood glucose test strips
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
cambridge sensorscambridge
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCHoneywell Recalls System Sensor L-Series Low Frequency Fire Alarm Sounders and Strobes Due to Risk of Failure to Alert Consumers to a Fire2024-03-14
- FDAIncisive CT Power- Whole-body computed tomography (CT) X-Ray System Model Number: 728148 (OUS)2023-04-12
- FDAIncisive CT Plus -Whole-body computed tomography (CT) X-Ray System Model Number: 728149 (OUS)2023-04-12
- FDAIncisive CT- Whole-body computed tomography (CT) X-Ray System Model Number: 728143 (OUS)2023-04-12
- FDAIncisive CT- whole-body computed tomography (CT) X-Ray System Model Number: 7281442023-04-12
- CPSCCambridge Elevating Residential Elevators Recalled Due to Child Entrapment Hazard; Risk of Serious Injury or Death to Young Children2022-09-29
- CPSCCambridge Elevating Recalls Home Elevators Due to Fall Hazard2019-03-27
- CPSCTerraTrike Recalls Adult Tricycles Due to Crash and Injury Hazards2018-12-18
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →