FDA recalling firm · 14 enforcement events · 16 product records · 2011–2020 · CA
Ormco/Sybronendo has 14 FDA enforcement events on this register (16 product records) between 2011 and 2020: 14 device; the busiest year was 2013 with 3.
0% of its events are Class I; the most common class is Class II (13). 0 events are listed as ongoing; the recalling firm's address is in CA.
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.
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
11
13
15
17
19
21
23
25
Enforcement events for Ormco/Sybronendo by year initiated.
Questions and answers
How many FDA recalls has Ormco/Sybronendo had?
14 enforcement events (16 product records) on this register, 2011–2020: 14 device.
Are any Ormco/Sybronendo recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are Ormco/Sybronendo recalls?
13 Class II, 1 Class III. 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.