JAS Diagnostics Inc.
JAS Diagnostics Inc. has 3 FDA enforcement events on this register (3 product records) between 2014 and 2017: 3 device; the busiest year was 2014 with 2.
0% of its events are Class I; the most common class is Class II (3). 0 events are listed as ongoing; the recalling firm's address is in FL.
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 |
|---|---|---|---|---|---|
| 21 Apr 2017 | Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent. | Device | Class II | 1 | Terminated |
| 23 Oct 2014 | Glucose Hexokinase (Liquid) Reagent For the in vitro quantitative determination of Glucose in serum. | Device | Class II | 1 | Terminated |
| 7 Apr 2014 | Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum. | Device | Class II | 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 JAS Diagnostics Inc. had?
3 enforcement events (3 product records) on this register, 2014–2017: 3 device.
Are any JAS Diagnostics Inc. recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are JAS Diagnostics Inc. recalls?
3 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.