National Biological Corp
National Biological Corp has 3 FDA enforcement events on this register (3 product records) between 2013 and 2017: 3 device; the busiest year was 2013 with 2.
0% of its events are Class I; the most common class is Class III (2). 0 events are listed as ongoing; the recalling firm's address is in OH.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 27 Jan 2017 | Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment. | Device | Class II | 1 | Terminated |
| 9 Apr 2013 | Dermalight 80 Model Number UVB-080, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo. | Device | Class III | 1 | Terminated |
| 8 Apr 2013 | Dermalight 80 Model Number UVB-083, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo. | Device | Class III | 1 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has National Biological Corp had?
3 enforcement events (3 product records) on this register, 2013–2017: 3 device.
Are any National Biological Corp recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are National Biological Corp recalls?
2 Class III, 1 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.