FDA Recall United States Terminated Historical recordClass I
ELITE CONFECTIONERY LTD
- Product
- Elite Hazelnut & Almond Milk Chocolate Bar Net Wt. 3.53 oz 1…
- Reason
- Potential contamination with Salmonella
- Published
- June 15, 2022
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,786
Class I recallsReasonable probability of serious health consequences24,313
Class II recallsTemporary or medically reversible health consequences2,876
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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.
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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 | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
FDA Recall Terminated Historical recordClass I
Anagrelide Capsules USP, 0.5 mg, 100-count bottles, Rx Only, Manufactured in India For: TEVA PHARMACEUTICALS USA, Inc., North Wales, PA 19454. NDC 0172-5241-60.
- Reason
- Failed Dissolution Specifications- Low Out-Of-Specification results obtained during stability testing.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollients, Net Wt. 5 oz (141 g), Distributed by Johnson & Johnson Consumer, Inc. Skillman, NJ 08558, UPC 3 81137-001530 7
- Reason
- cGMP deviations: product stored outside of labeled temperature requirements.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96536 9
- Reason
- cGMP deviations: product stored outside of labeled temperature requirements.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E Advanced Aloe Vera, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96537 6
- Reason
- cGMP deviations: product stored outside of labeled temperature requirements.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
AMBI Skincare Even & Clear Exfoliating Wash Salicylic Acid Acne Treatment With Oat and Sea Whip, Net Wt. 5 OZ. (141 g)
- Reason
- cGMP deviations: product stored outside of labeled temperature requirements.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
AMBI Skincare Fade Cream Normal Skin, Net Wt. 2 OZ. (56g)
- Reason
- cGMP deviations: product stored outside of labeled temperature requirements.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Only At Family Dollar AMBI Skincare Even & Clear Nourishing Daily Facial Moisturizer With Broad Spectrum SPF 30 Sunscreen, Net Wt. 1.7 FL. OZ. (50 mL)
- Reason
- cGMP deviations: product stored outside of labeled temperature requirements.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets, USP, 100 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816. 90 film coated tablets NDC 64380-935-05 1000 film coated tablets NDC 64380-935-08
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets, USP 25 mg, Rx only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816. 90 film coated tablets NDC 64380-933-05 1000 film coated tablets NDC 64380-933-08
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Equate Tartar Control Plus (Eucalyptol 0.092%, Menthol 0.042%, Methyl salicylate 0.060%, Thymol 0.064%) Antiseptic Mouthrise Plus, Antigingivitis/Antiplaque, Blue Mint, 1.5 Liter (50.7 FL OZ) bottle, Distributed By: Wal-Mart Stores, Inc., Bentonville, AR 72716, UPC 6 81131 14800 9
- Reason
- Superpotent Drug: product complaint for milky blue appearance and consistency, further investigation by the firm found the recalled lots out of specification for the four active ingredients.
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Succinylcholine Chloride Injection, USP, 100 mg/5 mL (20 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-920-05
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Rocuronium Bromide Injection, 50 mg/5 mL (10 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-924-05
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenylephrine HCl Injection, USP, 1 mg/10 mL (100 mcg/mL), 10 mL Pre-Filled Syringe, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-957-10
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenylephrine HCl Injection, USP, 0.8 mg/10 mL (80 mcg/mL), 10 mL Pre-Filled Syringes, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-956-10
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection, USP, 500 mL Single-Dose Container Bag, 10 x 1 IV Bag, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-543-50
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL), Preservative Free, 4 mL Pre-Filled Syringe, 5 x 4 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-946-04
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ketamine Hydrochloride Injection, USP, 30 mg/3 mL (10 mg/mL), 3 mL Pre-Filled Syringe, 5 x 3 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-982-33
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Hydromorphone HCl Injection, USP, 50 mg/50 mL (1 mg/mL), 50 mL Pre-Filled Syringe, 5 x 50 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-559-50
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Glycopyrrolate Injection, USP, 1 mg/5 mL (0.2 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-903-05
- Reason
- Lack of Assurance of Sterility
- Published
- June 8, 2022
- 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.
