Active Investigation 2026 record Source: FDA
Cyclosporiasis
- Cases
- 22
- Start date
- August 5, 2026
- Last updated
Health Alerts
Your unified view of current, active outbreak investigations, elevated disease activity, and food and drug recalls -- reported directly by CDC, FDA, and USDA. Not CDC NORS, which is a historical archive compiled well after an investigation closes (see Data Explorer for the full historical record).
Download matching alerts as CSV
CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.
Filters
FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL
- Announced by FDA
- August 5, 2026
FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Compounded Glutathione 200 mg/mL Multi-Dose Vials
- Announced by FDA
- August 5, 2026
Drug Recall 2026 record Source: FDA
Morphine Sulfate Injection, USP, 2 mg /mL, 1 mL single-dose Simplist prefilled syringes, For Intramuscular or Intravenous use, Rx only, Fresenius Kabi, Lake Zurich, IL. Unit of Use NDC Number 76045-004-01; Unit of Sale NDC Number 76045-004-11
- Recall initiated
- August 4, 2026
- Reported by FDA
- August 26, 2026
FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
OPTIRAY Imaging Bulk Package (IBP) 350, 500mL in vial (Ioversol Injection 74% 350 mg iodine/ml)
- Announced by FDA
- August 4, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Vegan Non-Dairy Frozen Dessert Coconut Fudge Sandwiches
- Announced by FDA
- August 4, 2026
Terminated
Drug Recall 2026 record Source: FDA
Clobetasol Propionate Cream USP, 0.05%, 60 g tube, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, United States, Manufactured by: Lupin Limited, Pithampur (MP) 454 775, INDIA, NDC 68180-956-04.
- Recall initiated
- August 3, 2026
- Reported by FDA
- September 2, 2026
Drug Recall 2026 record Source: FDA
Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Distributed by: Taro Pharmaceuticals USA, Inc., Hawthorne, NY 10532, NDC 51672-4005-3.
- Recall initiated
- August 3, 2026
- Reported by FDA
- August 26, 2026
FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Adequan Canine Injection and Adequan i.m Injection for horses
- Announced by FDA
- August 3, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Pistachio Nut Butter
- Announced by FDA
- August 3, 2026
Food Recall 2026 record Source: FDA
EURO FOODS GROUP USA NJ INC
- Recall initiated
- August 1, 2026
- Reported by FDA
- September 16, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Baked Spaghetti and Bread Pudding products
- Announced by FDA
- August 1, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Eridanous Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling 11.6 oz (330 g) box
- Announced by FDA
- July 31, 2026
Food Recall 2026 record Source: FDA
Ukrop's Homestyle Foods LLC
- Recall initiated
- July 30, 2026
- Reported by FDA
- September 9, 2026
Food Recall 2026 record Source: FDA
Ukrop's Homestyle Foods LLC
- Recall initiated
- July 30, 2026
- Reported by FDA
- September 9, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Aquafaba Powder 4oz (113g) and (12 oz (340g) flexible foil pouches
- Announced by FDA
- July 30, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Organic IQF Frozen Blueberries and Whole Mixed Berries, 10 oz and 48 oz
- Announced by FDA
- July 30, 2026
Terminated
Drug Recall 2026 record Source: FDA
PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2461-1
- Recall initiated
- July 29, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2453-1
- Recall initiated
- July 29, 2026
- Reported by FDA
- August 26, 2026
Food Recall 2026 record Source: FDA
Wonton Specialists
- Recall initiated
- July 28, 2026
- Reported by FDA
- September 9, 2026
Data last updated:
Investigations and recalls may be ongoing; status, case counts, and guidance are updated by the source agency as events continue. Read the full medical disclaimer.
