FDA Recall Completed Historical recordClass II
Altaire Sterile Eye Wash, 15 mL (1/2 fl oz), Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931 NDC 59390-175-13
- Reason
- Lack of Assurance of Sterility
- Published
- November 27, 2019
- Distribution
- Nationwide
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,115
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026
Download matching recalls as CSV
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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 Completed Historical recordClass II
Altacaine (Tetracaine Hydrochloride) Ophthalmic Solution, USP, 0.5%, 15 mL, Rx only, Mfd. by: Altaire Pharmaceuticals Inc. Aquebogue, NY 111931, NDC 59390-181-13
- Reason
- Lack of Assurance of Sterility
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Completed Historical recordClass II
Perrigo Neomycin and Polymixin B Sulfates and Dexamethasone Ophthalmic Ointment, Net. Wt 3.5 gm, Sterile, Rx only, Manufactured for Perrigo Minneapolis, MN 55427, NDC 0574-4160-35
- Reason
- Lack of Assurance of Sterility
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Levetiracetam Injection, 500 mg/5mL, 10 single-use 5 mL vials, Rx only, Manufactured by: Agile Specialties Private Limited Pilot No. 14, Sipcot II, Hosur-635 109 Tamil Nadu, India, Manufactured for: X-Gen Pharmaceuticals, Inc. Big Flats, NY 14814, NDC 39822-4000-1
- Reason
- Labeling: Incorrect or Missing Package Insert - the incorrect package insert version was attached.
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
0.9% Sodium Chloride Irrigation USP 5000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0047-29
- Reason
- Lack of Assurance of Sterility: Product has the potential to leak.
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 2.5mg / Ipratropium 0.75mg/ Triamcinolone 0.5 mg 3ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 1.25mg / Ipratropium 0.5mg, 2ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 1.25mg / Ipratropium 0.5mg/ Budesonide 0.25mg, 3ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 2.5mg / Budesonide 0.5mg, 3ML Vial, For Inhalation Only, Shake Well, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 2.5mg / Ipratropium 0.75mg /Budesonide 0.25mg, 3ML Vial, For Inhalation Only, Shake Well, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 2.5mg / Ipratropium 0.75mg /Budesonide 0.5mg, 3ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 2.5mg / Ipratropium 0.75mg, 2ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Albuterol 3.75mg / Ipratropium 0.75mg, 3ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Budesonide 0.4mg, 3ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Formoterol 12mcg / Budesonide 0.5mg, 3.5ML Vial, For Inhalation Only, Shake Well, Conversio Health, San Luis Obispo, CA 93401.
- Reason
- Lack of Processing Controls
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
R2103, Active Ingredients: Berberis Aquifolium 3x; Borax 3; , Kreosotum 10X; Sepia 3x. Inactive ingredient: 28% dilution alcohol, packaged in a) 470 mL bottle and b) 1000 mL bottle; Manufactured for Wisconsin Pharmacal Company, By: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
- Reason
- CGMP Deviations: products were not manufactured under current good manufacturing practices.
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
StellaLife VEGA Oral Gel Rinse (In equal parts of: Azadirachta Indica 1x, Calendula Officinalis 1x, Echinacea Purpurea 1x, Plantago Major 1x), packaged in 1000 mL white plastic bottle.
- Reason
- CGMP Deviations: products were not manufactured under current good manufacturing practices.
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Silicea 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64199 6.
- Reason
- CGMP Deviations: products were not manufactured under current good manufacturing practices.
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Natrum Sulphuricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64193 4.
- Reason
- CGMP Deviations: products were not manufactured under current good manufacturing practices.
- Published
- November 27, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Natrum Phosphoricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64192 7.
- Reason
- CGMP Deviations: products were not manufactured under current good manufacturing practices.
- Published
- November 27, 2019
- 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.
