PQ Corporation FDA Record
PQ Corporation has 1 FDA recall, 12 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "PQ Corporation" is on file.
- Latest recall
- D-0564-2016 · Class III · Oct 29, 2015
- Latest inspection
- Apr 15, 2025 · NAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 1 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 12 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
FDA record by year
| Year | Inspections | OAI | Warning letters | Recall records | Class I |
|---|---|---|---|---|---|
| 2026 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 1 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 2 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 1 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2017 | 1 | 0 | 0 | 0 | 0 |
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Recent recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-0564-2016 | Class III | EPSOM SALT(Magnesium Sulfate Heptahydrate, USP), 50 lb multi-wall bag, Rx only, Manufactured by PQ… | Oct 29, 2015 |
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Apr 15, 2025 | Joliet, IL | Food/Cosmetics | No Action Indicated (NAI) | 1000114852 |
| Jun 27, 2022 | Saint Louis, MO | Food/Cosmetics | No Action Indicated (NAI) | 3004311208 |
| Feb 22, 2022 | Utica, IL | Veterinary | Voluntary Action Indicated (VAI) | 1421453 |
| Apr 16, 2019 | Utica, IL | Drugs | Voluntary Action Indicated (VAI) | 1421453 |
| May 31, 2017 | Utica, IL | Veterinary | Voluntary Action Indicated (VAI) | 1421453 |
| Jun 14, 2016 | Saint Louis, MO | Food/Cosmetics | No Action Indicated (NAI) | 3004311208 |
| Apr 18, 2016 | Utica, IL | Drugs | Voluntary Action Indicated (VAI) | 1421453 |
| Jun 17, 2015 | Avenel, NJ | Food/Cosmetics | No Action Indicated (NAI) | 3004056935 |
| Dec 19, 2013 | Utica, IL | Drugs | Voluntary Action Indicated (VAI) | 1421453 |
| Sep 13, 2012 | Avenel, NJ | Drugs | No Action Indicated (NAI) | 3004056935 |
| Aug 2, 2011 | Utica, IL | Drugs | Voluntary Action Indicated (VAI) | 1421453 |
| May 6, 2010 | Utica, IL | Drugs | No Action Indicated (NAI) | 1421453 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 1000114852 | Joliet, IL | 1 | Apr 15, 2025 |
| FEI 3004311208 | Saint Louis, MO | 2 | Jun 27, 2022 |
| FEI 1421453 | Utica, IL | 7 | Feb 22, 2022 |
| FEI 3004056935 | Avenel, NJ | 2 | Jun 17, 2015 |
PQ Corporation and the FDA: common questions
Has PQ Corporation received an FDA warning letter?
No FDA warning letter addressed to the name "PQ Corporation" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has PQ Corporation received an FDA Form 483?
FDA has not published a Form 483 for "PQ Corporation" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect PQ Corporation?
The most recent FDA inspection on file ended Apr 15, 2025 at Joliet, IL and was classified NAI. FDA has 12 inspections of PQ Corporation on file.
Has PQ Corporation had an FDA recall?
Yes. PQ Corporation has 1 FDA recall on record. The most recent started Oct 29, 2015.
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