FDA Device recall Z-1339-2016
Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL), Black
- FDA Device
- Class I
- terminated
- Published 2016-04-20
On 2016-04-20 the FDA classified a Class I recall of Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL), Black by Dexcom, citing customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1339-2016 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-02-23 |
| Published | 2016-04-20 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Dexcom |
| Distribution | US |
Product
Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL), Black; MT22719-PNK, Receiver (mg/dL), Pink; MT22719-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.
Reason
Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.
Identifiers
| code_info | Receiver Kit Number: STK-GF-001 STK-RF-001 STR-GF-001 STK-GF-PNK STK-RF-PNK STR-GF-PNK STK-GF-BLU STK-RF-BLU S…Receiver Kit Number: STK-GF-001 STK-RF-001 STR-GF-001 STK-GF-PNK STK-RF-PNK STR-GF-PNK STK-GF-BLU STK-RF-BLU STR-GF-BLU Lot Number: 5204518 5204520 5204526 5204529 5204546 5204644 5204647 5204697 5204752 5204756 5204760 5204764 5204941 5204959 5204995 5205003 5205015 5205024 5205039 5205057 5205059 5206564 5206577 5206601 5206618 5206630 5206724 5207977 5207978 5207983 5207994 5208000 5208001 5208013 5208014 5208017 5208026 5208027 5208030 5208034 5208263 5208264 5208349 5208350 5208512 5208515 5208524 5208525 5208799 5208803 5208817 5209310 5209311 5209313 5209657 5209660 5210388 5210468 5204519 5204525 5204528 5204545 5204645 5204648 5204698 5204754 5204758 5204952 5205007 5205029 5205050 5206565 5206576 5206606 5206623 5207980 5207987 5207996 5208009 5208513 5208523 5208815 5209314 5209317 5209319 5209658 5209661 5210391 5204521 5204527 5204530 5204646 5204699 5204757 5204761 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1339-2016%22
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