Recall Z-2295-2019— Arcos, Inc
Class II · Terminated
Class II FDA medical device recall by Arcos, Inc, initiated 2015-03-16, terminated 2022-02-09. Product: 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: Panasonic Model CF-H2 Part Number CMP-1523. Reason: Battery packs may heat up abnormally and ignite in rare instance..
- Recalling firm
- Arcos, Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-03-16
- Terminated
- 2022-02-09
- Firm location
- Missouri City, TX, United States
Product description
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: Panasonic Model CF-H2 Part Number CMP-1523
Reason for recall
Battery packs may heat up abnormally and ignite in rare instance.
Data sourced from openFDA. This site is unofficial and independent of the FDA.