Severity
Moderate
FDA Devices recall · Reported August 28, 2019
Battery packs may heat up abnormally and ignite in rare instance.
Arcos, Inc recalled Brand Name Burn Navigator¿ Model Numbers: Catalog 1120, Burn Navigator¿ H2 Catalog 112… - a moderate-severity action.
Brand Name Burn Navigator¿ Model Numbers: Catalog 1120, Burn Navigator¿ H2 Catalog 112… was recalled by Arcos, Inc in August 28, 2019. Reason: Battery packs may heat up abnormally and ignite in rare instance.. Check the official notice for the remedy. Verify recall #Z-2295-2019 with the FDA Devices before acting.
The recall
Arcos, Inc issued this moderate-severity FDA Devices recall-Battery packs may heat up abnormally and ignite in rare instance..
Sourced from official FDA Devices enforcement records. Verify recall #Z-2295-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-2295-2019) was formally reported on August 28, 2019, with the manufacturer initiating the action on March 16, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Arcos, Inc is listed as the recalling firm, operating out of Missouri City, TX. Federal records list the affected scope as 28.
The documented reason for this recall is: Battery packs may heat up abnormally and ignite in rare instance. Distribution data in the federal record shows the product reached: US: AZ, LA, OR, MD, TX, and WA. OUS: No products were distributed outside the US.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
28
Related Recalls
6
3 from same agency
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
Battery packs may heat up abnormally and ignite in rare instance.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2295-2019 |
| Date reported | August 28, 2019 |
| Date initiated | March 16, 2015 |
| Recalling firm | Arcos, Inc |
| Firm location | Missouri City, TX |
| Affected scope | 28 |
| Distribution | US: AZ, LA, OR, MD, TX, and WA. OUS: No products were distributed outside the US. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported August 28, 2019. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.