NOMAD Pro2 Packaged X-Ray System — Class II medical device recall Z-2717-2016
Terminated recall by Aribex Inc, reported 2016-09-14, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Firm received customer complaints where end users reported that Nomad Pro and Pro 2 handsets had appeared to "
| Recall number | Z-2717-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aribex Inc, Charlotte, NC, United States |
| Recall initiated | 2016-07-18 |
| Classified | 2016-09-02 |
| Reported by FDA | 2016-09-14 |
| Terminated | 2017-07-26 |
| Distributed | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
| Countries outside the US | AE, AF, AR, AU, BE, BH, BM, BS, CH, CL, CN, DE, DK, FI, FR, GB, GR, GT, HK, HU, ID, IE, IL, IN, IQ, IT, JM, JP, KW, MA, MX, MY, NL, NZ, PH, PL, QA, SA, SE, SI, TH, TR, TT, VE, VN, ZA |
| Quantity | 16,871 |
| Reason classes | device malfunction |
| Model numbers | 08500021, 08500022, 08500023, 08500024, 08500025, 08500026, 08500027, 08500028, 08500029 |
Product
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 08500025 and Part Number 08500026; NOMAD Pro2 Packaged X-Ray System, GLB, Vet, Part Number 08500027 and Part Number 08500028; NOMAD Pro2 Package X-Ray System, GLB, Black, Part Number 08500029
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2717-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.