Food Recall 2026 record Source: FDA
Saint Francis Apizza LLC
- Recall initiated
- October 1, 2026
- Reported by FDA
- October 14, 2026
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).
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FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Glutathione Injection
- Announced by FDA
- October 1, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Pasta
- Announced by FDA
- October 1, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Monterey Jack, Jalapeno Jack, Medium Cheddar, and Sharp Cheddar raw milk cheeses
- Announced by FDA
- September 29, 2026
Drug Recall 2026 record Source: FDA
Lidocaine Ointment USP, 5% (Generic for Xylocaine), packaged in a 50 g jar, Rx only, Mfg: Taro Pharmaceuticals U.S.A., Inc., Prod# (NDC): 68788-7865-05
- Recall initiated
- September 28, 2026
- Reported by FDA
- October 14, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Greek peppers/ Golden Greek Peperoncini, Medium Heat
- Announced by FDA
- September 26, 2026
Drug Recall 2026 record Source: FDA
Tretinoin Cream UPS, 0.05%, 20g, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals USA Inc., Hawthorne, NY 10532, NDC 51672-1394-0.
- Recall initiated
- September 25, 2026
- Reported by FDA
- October 14, 2026
Drug Recall 2026 record Source: FDA
Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Product of Canada, NDC 16714-249-02.
- Recall initiated
- September 25, 2026
- Reported by FDA
- October 14, 2026
Drug Recall 2026 record Source: FDA
Tretinoin Cream USP, 0.05%, 45g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals USA Inc., Hawthorne, NY 10532, NDC 51672-1394-9.
- Recall initiated
- September 25, 2026
- Reported by FDA
- October 14, 2026
Food Recall 2026 record Source: FDA
Pepsico Inc
- Recall initiated
- September 25, 2026
- Reported by FDA
- October 14, 2026
Drug Recall 2026 record Source: FDA
Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vial, Rx Only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC, 27513, NDC 85091-011-06.
- Recall initiated
- September 24, 2026
- Reported by FDA
- October 14, 2026
Drug Recall 2026 record Source: FDA
Tirzepatide Injection, 18mg/mL, 4 mL Sterile Multi-Dose Vial, Rx only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC 27513, NDC 85091-001-18.
- Recall initiated
- September 24, 2026
- Reported by FDA
- October 14, 2026
Food Recall 2026 record Source: FDA
GIAS FOOD INC.
- Recall initiated
- September 24, 2026
- Reported by FDA
- October 14, 2026
Food Recall 2026 record Source: FDA
Galil Importing Corp
- Recall initiated
- September 24, 2026
- Reported by FDA
- October 7, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Ground cinnamon
- Announced by FDA
- September 24, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Pasta
- Announced by FDA
- September 24, 2026
Drug Recall 2026 record Source: FDA
IMAAVY (nipocalimab-aahu) Injection, 300 mg /1.62 mL (185 mg/mL) per single-dose vial, For Intravenous Infusion After Dilution, Rx only, Manufactured by: Janssen Biotech, Inc., Horsham, PA 19044. NDC: 57894-800-01
- Recall initiated
- September 23, 2026
- Reported by FDA
- October 14, 2026
Drug Recall 2026 record Source: FDA
Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-1318-3
- Recall initiated
- September 23, 2026
- Reported by FDA
- October 7, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Alfalfa sprouting seeds
- Announced by FDA
- September 23, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Organic Unsweetened Apple Sauce
- Announced by FDA
- September 22, 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.
