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

Recall Z-2717-2016 — NOMAD Pro2 Packaged X-Ray System, Part Number 08500021; NOMAD Pro2 Packaged X-Ray System Black, Part Number 08500022; NOMAD Pro2 Vet Packaged X-Ray System, Part Number 08500023; NOMAD Pro2 Vet Packaged X-Ray System Black, Part Number 08500024; NOMAD Pro2 Packaged X-Ray System, GBL, Part Number 08500

U.S. FDA — Device Enforcement · United States · 2016-07-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2717-2016
Date of alert: 2016-07-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Aribex Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 08500021

Reported risk: Firm received customer complaints where end users reported that Nomad Pro and Pro 2 handsets had appeared to "overheat", "melt", "smoke" and/or "ignite." Investigation found that the internal lithium ion batteries had entered into a thermal runaway condition as a result of a short circuit on the battery pack PCB.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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