Missouri City, TX, United States
Arcos, Inc recalls
1 recall recorded since 2018, most recently on 16 March 2015. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 16 March 2015
- Terminated
- 9 February 2022
- Reason
- Battery packs may heat up abnormally and ignite in rare instance.
- Distribution
- US: AZ, LA, OR, MD, TX, and WA. OUS: No products were distributed outside the US.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2295-2019
- Brand Name Burn Navigator¿ Model Numbers: Catalog 1120, Burn Navigator¿ H2 Catalog 1125, Burn Navigator¿ H2 Transport Package Burn Navigator User Manual Manual-1120 Burn Navigator User's Manual, Rev. F Battery:
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.