Food Recall 2026 record Source: FDA
Taylor Farms de Mexico S. de R.L. de C.V.
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 19, 2026
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Food Recall 2026 record Source: FDA
Taylor Farms de Mexico S. de R.L. de C.V.
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 19, 2026
Food Recall 2026 record Source: FDA
Taylor Farms de Mexico S. de R.L. de C.V.
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 19, 2026
Food Recall 2026 record Source: FDA
Taylor Farms de Mexico S. de R.L. de C.V.
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 19, 2026
Food Recall 2026 record Source: FDA
Taylor Farms de Mexico S. de R.L. de C.V.
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 19, 2026
Food Recall 2026 record Source: FDA
Taylor Farms de Mexico S. de R.L. de C.V.
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 19, 2026
Drug Recall 2026 record Source: FDA
Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 12, 2026
Drug Recall 2026 record Source: FDA
Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1
- Recall initiated
- July 17, 2026
- Reported by FDA
- August 12, 2026
CDC Announcement 2026 record Source: CDC
Cyclospora Outbreak Linked to Iceberg Lettuce
- Start date
- July 17, 2026
- Last updated
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Pounded Yam (2lb, 4lb, 5lb, 10 lb)
- Announced by FDA
- July 17, 2026
Drug Recall 2026 record Source: FDA
Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound Volume 416.8 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Inc., Atlanta, 1750 Corp Dr. Ste 725, Norcross, GA 30093 (844) 903-6418
- Recall initiated
- July 16, 2026
- Reported by FDA
- August 12, 2026
Drug Recall 2026 record Source: FDA
Dabigatran Etexilate Capsules, 75 mg, 30-count (3x10) blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268, NDC 0904-7253-04.
- Recall initiated
- July 16, 2026
- Reported by FDA
- August 5, 2026
Drug Recall 2026 record Source: FDA
Dabigatran Etexilate Capsules, 75 mg, 60-count (6x10)blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268, NDC 0904-7253-68.
- Recall initiated
- July 16, 2026
- Reported by FDA
- August 5, 2026
Drug Recall 2026 record Source: FDA
Dabigatran Etexilate Capsules, 150 mg, 60-count (6x10) blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268, NDC 0904-7255-68.
- Recall initiated
- July 16, 2026
- Reported by FDA
- August 5, 2026
Food Recall 2026 record Source: FDA
CHEER PACK
- Recall initiated
- July 16, 2026
- Reported by FDA
- August 12, 2026
Drug Recall 2026 record Source: FDA
Xylocaine (lidocaine HCl Injection, USP), 1%, 500 mg per 50 mL (10 mg per mL), 25 Multiple-Dose Vials, 50 mL, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-485-57; NDC Vial: 63323-485-03
- Recall initiated
- July 16, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
Xylocaine (lidocaine HCl Injection, USP), 1%, 200 mg per 20 mL (10 mg per mL), 25 Multiple-Dose Vials, 20 mL, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-485-27; NDC Vial: 63323-485-01
- Recall initiated
- July 16, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
Naropin (ropivacaine hydrochloride Injection, USP), 0.5%, 100 mg per 20 mL (5 mg per mL), Twenty-five, 20 mL Single-Dose Vials, Rx only, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-286-23; NDC Vial: 63323-286-05
- Recall initiated
- July 16, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-208-05; NDC Vial: 63323-208-01
- Recall initiated
- July 16, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
Glycopyrrolate Injection, USP, 1 mg per 5 mL (0.2 mg per mL), 25 x 5 mL fill in a 6.5 mL vial, Rx only, Multiple Dose Vials, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-578-05; NDC Vial: 63323-578-07
- Recall initiated
- July 16, 2026
- Reported by FDA
- July 29, 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.
