Medtronic Guardian Sensor 3 Recalled for Inaccurate Glucose Readings
Medtronic is recalling Guardian Sensor 3 units worldwide because use with hydroxyurea may cause inaccurate elevated glucose readings.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device where a specific drug interaction (hydroxyurea) can cause inaccurate readings, posing a risk of harm to patients with diabetes, but no specific injuries or illnesses are reported in the source text.
Plain-English summary
Medtronic Inc. is recalling 68,069 units of the Guardian Sensor (3) (REF: MMT-7020C5) for worldwide distribution. The recall involves specific packaging configurations (GS3 5PK 1L AUS) with GTINs 20763000252056 and 20763000414362. The product is intended for use with Medtronic Diabetes glucose sensing systems to continuously monitor glucose levels in persons with diabetes.
The recall was initiated because using the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug, could result in inaccurate elevated sensor glucose readings. The source text notes that the product was not distributed within the US.
Consumers and healthcare providers should stop using the affected sensors if they are actively taking hydroxyurea and consult their healthcare provider regarding alternative glucose monitoring methods. The recall covers all lot numbers within the active shelf life.
The recalled product
- Product
- Medtronic REF: MMT-7020C5 Guardian Sensor (3) for the following packaging: GS3 5PK 1L AUS/ GTIN: 20763000252056 GS3 5PK 1L AUS/ GTIN: 20763000414362 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose
- Manufacturer
- Medtronic Inc.
- Affected units
- 68,069
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All Lot numbers within active shelf life
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 20 recalled by Medtronic Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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