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

Recall Z-2528-2018 — Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model 087.4010); b. 15 Days Negative Pressure Wound Therapy (Model 087.4012); c. 60 Days Negative Pressure Wound Therapy (Model 087.4014); d. Endure Negative Pressure Wound Ther

U.S. FDA — Device Enforcement · United States · 2018-02-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2528-2018
Date of alert
2018-02-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medela Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
16611001
Reported risk: Device may display a battery missing error.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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