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

Recall Z-1820-2012 — USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Models AT3800 and AT4700. Brochure: "EXER-REST***A patented, FDA registered, Acceleration T

U.S. FDA — Device Enforcement · United States · 2012-05-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1820-2012
Date of alert
2012-05-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Non-Invasive Monitoring Systems, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
305357534201
Reported risk: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling promotional materials which contain unsubstantiated direct and indirect claims.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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