FDA Recall United States Terminated Historical recordClass II
Snapchill, LLC
- Product
- Black Coffee + Sweet Syrup Canned Beverage packaged under th…
- Reason
- Potential under-processing.
- Published
- July 24, 2024
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,061
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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 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 United States Terminated Historical recordClass II
Snapchill, LLC
- Product
- Black Coffee + Chocolate Syrup and Sugar Canned Beverage pac…
- Reason
- Potential under-processing.
- Published
- July 24, 2024
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Snapchill, LLC
- Product
- Black Coffee + Chocolate Syrup Canned Beverage packaged unde…
- Reason
- Potential under-processing.
- Published
- July 24, 2024
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Snapchill, LLC
- Product
- Black Coffee + Sugar Canned Beverage packaged under the foll…
- Reason
- Potential under-processing.
- Published
- July 24, 2024
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Snapchill, LLC
- Product
- Black Coffee Canned Beverage packaged under the following br…
- Reason
- Potential under-processing.
- Published
- July 24, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Diflorasone Diacetate Ointment, USP, 0.05%, 60g tube, Rx only, Mfd. By: Lyne Laboratories, Inc., Brockton, MA 02301; Mfd. For: Rising Pharmaceuticals, Inc., East Brunswick, NJ 08816 NDC 64980-124-60
- Reason
- Failed Impurities/Degradation Specifications: The impurity results at 12 months stability testing,did not conform to the specification limit.
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Completed Historical recordClass III
Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, NDC 16714-301-01 (vial), NDC 16714-301-10 (outer box).
- Reason
- Cross contamination with other products
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Completed Historical recordClass III
Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1725-01 (vial), NDC 70710-1725-06 (outer box).
- Reason
- Cross contamination with other products
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2
- Reason
- Subpotent Drug: reduced efficacy for epinephrine
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534, Vial NDC: 70710-1644-1, Carton NDC: 70710-1644-5.
- Reason
- Cross contamination with other products.
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Verapamil Hydrochloride Injection, USP 5 mg / 2mL(2.5 mg/mL), packaged as (a) 25x2 mL Single-Dose Vial per carton, Vial NDC: 70710-1643-1; Carton NDC 70710-1643-7; (b) 5x2 mL Single-Dose Vial per carton, Vial NDC: 70710-1643-1; Carton NDC 70710-1643-5; Rx Only, Manufactured by: Zydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534,
- Reason
- Cross contamination with other products.
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Blemfree All Day Lotion (salicylic acid 0.5% w/w), packaged in a) 1 oz. 29 ML tube NDC:53228-003-01 b) 4 OZ 118ML plastic bottle, UPC 7 01450 90008 6, NDC # 53228-002-01, Equibal Labs, Inc
- Reason
- CGMP Deviations: Manufactured without following Current Good Manufacturing Practises.
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC: 60687-782-01.
- Reason
- Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
suntegrity, (Zinc Oxide 15%) IMPECCABLE SKIN sunscreen foundation, Multiple Shades, Broad Spectrum SPF30, Net WT 2OZ (56.7 g), Suntegrity Skincare, Las Vegas, NV 89128, a) NDC: 69949-151-01, UPC: 854245006170 - IVORY b) NDC: 69949-156-01, UPC: 854245006224 - NUDE c) NDC: 69949-152-01, UPC: 854245006187 - BUFF d) NDC: 69949-153-01, UPC: 854245006194 - SAND e) NDC: 69949-155-01, UPC: 854245006217 - BRONZE f) NDC: 69949-157-01, UPC: 854245006446 - MOCHA
- Reason
- CGMP Deviations
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
suntegrity, (Zinc Oxide 15%) IMPECCABLE SKIN sunscreen foundation, BUFF, Broad Spectrum SPF30, Net WT 2OZ (56.7 g), Suntegrity Skincare, Las Vegas, NV 89128, NDC: 69949-152-01 UPC 854245006187
- Reason
- Microbial Contamination of Non-Sterile Products: Presence of Aspergillus Sydowii (Mold)
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, For Intraperitoneal Administration Only, 6000 mL per bag, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA. NDC: 0941-0457-01
- Reason
- Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component.
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
fgf brands, inc
- Product
- Bakeshop Chocolate Chip Muffin 4 count, in clear plastic cla…
- Reason
- Undeclared Walnut
- Published
- July 17, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
To the Moon Capsules, Horny Goat Weed, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
- Reason
- Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
- Published
- July 10, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
- Reason
- Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
- Published
- July 10, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Venlafaxine Hydrochloride, extended-release capsules, USP, 37.5mg, 10 x 10 blister card in one carton, Rx only, Mfg by: Cadila Healthcare Ltd., Ahmedabad, India, Distributed by: Major Pharmaceutical 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, USA, NDC 0904-7075-61, UPC code: 309047075614
- Reason
- Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.
- Published
- July 10, 2024
- 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.
