Johnson Matthey Inc.
Johnson Matthey Inc. has 3 FDA enforcement events on this register (5 product records) between 2018 and 2019: 3 drug; the busiest year was 2019 with 2.
0% of its events are Class I; the most common class is Class II (2). 0 events are listed as ongoing; the recalling firm's address is in NJ.
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 |
|---|---|---|---|---|---|
| 29 Aug 2019 | Fentanyl Citrate Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001. | Drug | Class II | 3 | Terminated |
| 2 Apr 2019 | Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing, processing or repackaging, 416.95 g glass container, Rx ONLY, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742. | Drug | Class III | 1 | Terminated |
| 5 Mar 2018 | Morphine Sulfate USP Milled, Active Pharmaceutical Ingredient, Rx only, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742 | Drug | 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 Johnson Matthey Inc. had?
3 enforcement events (5 product records) on this register, 2018–2019: 3 drug.
Are any Johnson Matthey Inc. recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are Johnson Matthey Inc. recalls?
2 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.