FDA Recall Terminated Historical recordClass II
Calcium Gluconate1% Eyewash 10 mg/mL, 125 mL bottles, Pharm D Solutions, Houston, Texas ---- NDC 69699-0906-12
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
Data Explorer
Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.
Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,793
Class I recallsReasonable probability of serious health consequences24,343
Class II recallsTemporary or medically reversible health consequences2,887
Class III recallsNot likely to cause adverse health consequencesQuick insights
A snapshot of the most notable patterns across all recorded FDA and USDA recalls.
Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
53 recalls
Most common hazardLack of Assurance of Sterility
2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026
Download matching recalls as CSV
CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.
Filters
Metric
View
A chart of recalls grouped by month.
Download CSVSummary (Year to date)
- 1,527 recalls have been announced year to date.
- Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
- The highest complete period was Jun 2026 (297).
- Sep 2026 is incomplete and not included in the figures above.
- Complete data
- Incomplete
A bar chart of the total number of recalls in this dataset by recall class.
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
FDA Recall Terminated Historical recordClass II
Calcium Gluconate 1% Eyewash Oph. Soln, 10 mg/mL, 1000 mL bottles, Pharm D Solutions, Houston, Texas ---- NDC 69699-0907-10
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Caffeine and Sodium Benzoate Injection 125 mg/125 mg/mL Injectable Pharm D Solutions, Houston, Texas ---- NDC 69699-1428-02
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Bi-Mix (Papaverine/Phentolamine 150 mg/5 mg) a) Injectable NDC 69699-1760-15; b) (LYO) Powder NDC 69699-1760-15, Pharm D Solutions, Houston, Texas
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Bi-Mix Injection (Alprostadil 80 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1317-03
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Bi-Mix Injection, (Alprostadil 40 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1305-03
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Bi-Mix Injection (Alprostadil 150 mcg/Lidocaine 2 mg/mL), Pharm D Solutions, Houston, Texas --- NDC 69699-1323-05
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Bacteriostatic Water for Injection 10 mL, Pharm D Solutions, Houston, Texas --- NDC 69699-1417-10
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Beta-complex B-1, B-6, B-3, B-12, B-5 100, 2.54 Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1611-30
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ascorbic Acid 500 mg/mL Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1502-50
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Arginine Injections 100 mcg/mL, Pharm D Solutions, Houston, Texas NDC 69699-1414-20
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Acetylcysteine Injection 10 mg/5 mL (2 mg/mL), Pharm D Solutions, Houston, Texas ---- NDC 69699-1424-10
- Reason
- Lack of Assurance of Sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenylephrine 30 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Reason
- Lack of assurance of sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenylephrine 25 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Reason
- Lack of assurance of sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Hydromorphone (0.2 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Reason
- Lack of assurance of sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Fentanyl (10 mcg/mL) in NS 1 mL (in 3mL BD Syringe), Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Reason
- Lack of assurance of sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Morphine (1 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Reason
- Lack of assurance of sterility
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Catapres .2 (clonidine hydrochloride, USP) 0.2mg, 100-count bottles, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA. Made in Germany. NDC 0597-0007-01
- Reason
- Failed Dissolution Specifications: OOS resultsduring routine stability testing
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Diet Power, Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0004-1
- Reason
- CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
- Published
- November 7, 2018
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Body Balance, Homeopathic Oral Spray 1.38 fl. oz (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0039-1
- Reason
- CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
- Published
- November 7, 2018
- Distribution
- Nationwide
Data last updated:
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.
