Hand Foot II — Class II medical device recall Z-1683-2017
Terminated recall by National Biological Corp, reported 2017-04-05, distributed in IA, IL, MI, NY, PA, WI. The wiring may allow the lamps to turn on with the key switch rather than the timer.
| Recall number | Z-1683-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | National Biological Corp, Beachwood, OH, United States |
| Recall initiated | 2017-01-27 |
| Classified | 2017-03-24 |
| Reported by FDA | 2017-04-05 |
| Terminated | 2019-02-08 |
| Distributed | IA, IL, MI, NY, PA, WI |
| Countries outside the US | CA, JO, MX |
| Quantity | 7 units |
| Serial numbers | 39866, 39867, 39869, 39870, 39871, 39873, 39874 |
Product
Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment.
Reason for recall
The wiring may allow the lamps to turn on with the key switch rather than the timer.
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-1683-2017. 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.