Reported Apr 20, 2016 · Terminated

Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430 Receiver (mg/dL), Black (pediatrics);…

Dexcom Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Dexcom Inc · 6340 Sequence Dr · San Diego, CA · 92121-4356

Is this the product you have?

4 of 4 products

Products covered by this recall
Model / numberProduct as published
MT22430Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Receiver (mg/dL), Black (pediatrics)
MT22430-PNK, Receiver (mg/dL), Pink (pediatrics)
MT22430-BLU, Receiver (mg/dL)
Blue (pediatrics). Intended to detect trends and track glucose patterns in persons with diabetes.
Lot codes and dates
  • Receiver Kit NumberSTK-KD-001 STK-KX-001 STR-KD-001 STK-KD-PNK STK-KX-PNK STR-KD-PNK STK-KD-BLU
  • STK-KX-BLU STR-KD-BLU Lot Number

    223 of 223 codes

    • 5120310
    • 5135364
    • 5135371
    • 5136498
    • 5150416
    • 5150452
    • 5159486
    • 5166429
    • 5166430
    • 5178449
    • 5179449
    • 5187476
    • 5189594
    • 5190724
    • 5191132
    • 5191133
    • 5191174
    • 5191809
    • 5191810
    • 5191849
    • 5192890
    • 5194119
    • 5194120
    • 5194121
    • 5194431
    • 5195411
    • 5195746
    • 5195763
    • 5195776
    • 5195784
    • 5196133
    • 5196159
    • 5197032
    • 5197033
    • 5197647
    • 5120312
    • 5135362
    • 5135368
    • 5135380
    • 5136502
    • 5139380
    • 5150418
    • 5150454
    • 5153433
    • 5159487
    • 5166433
    • 5166449
    • 5166450
    • 5171430
    • 5178418
    • 5178456
    • 5179453
    • 5187474
    • 5189590
    • 5190725
    • 5191105
    • 5191134
    • 5191135
    • 5191408
    • 5191839
Amount recalled
18,004

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 11, 2017 · Data as of Sep 19, 6:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.