Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1335-2016 — Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430 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.

U.S. FDA — Device Enforcement · United States · 2016-02-23 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1335-2016
Date of alert
2016-02-23
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Dexcom Inc
Product category
device
Product type
Devices
Reported risk: Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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