8 food recalls and 8 new federal notices, most for other

Food recalls in the latest FDA reports

• 8food recalls
• 3Class I, the most serious
• 0labeled organic
• 1allergen mentions

1. Evergreen Fresh Sprouts LLCMoyie Springs, IDClass I

   Evergreen Fresh Sprouts LLC, Broccoli Sprouts, packaged in clear plastic zip lock bag, net wt. 4oz, UPC 8 38796 00105 1. Firm distributed cases (6/4oz. bags per case) to distributor.

   Reason: Salmonella

   FDA recall H-1390-2026, reported 2026-09-30, ongoing

2. Gias Food Inc.New York, NYClass I

   Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 20 2027 L6080C, UPC...

   Reason: Contamination with Listeria monocytogenes

   FDA recall H-1396-2026, reported 2026-09-30, ongoing

3. Wfm Purchasing, LpAustin, TXClass I

   Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life: 30 days, all dates through and including 10/7/2026 Packaging: Plastic wrapped by slice Net Wt.: Various, cut from whole wheel and priced by weight with Whole Foods...

   Reason: Undeclared Egg Allergen

   FDA recall H-1395-2026, reported 2026-09-30, ongoing

4. Elegant Foods, LLCMadison, WIClass II

   Pecorino Toscano D.O.P. STAGIONATO cheese wheels. Product of Italy. Each cheese wheel is approximately 3-4 lbs. Wheels contain a wax rind. Keep Refrigerated. Produced by Soc. Cooperativa Val D'Orcia Aocieta Agricola

   Reason: Potential Listeria contamination from dripping condensation in cooler.

   FDA recall H-1389-2026, reported 2026-09-30, ongoing

5. United Sugar Producers And RefinersMinneapolis, MNClass II

   Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051. Distributed By: United Sugar Producers & Refiners, Minneapolis, MN 55439. 2. Good & Gather, Net Wt 2 lb. (32 oz) 907g....

   Reason: Potential Wheat Kernel contamination.

   FDA recall H-1391-2026, reported 2026-09-30, ongoing

6. United Sugar Producers And RefinersMinneapolis, MNClass II

   Powdered Sugar, Packaged in the following configurations: 1. United 6X, Net Wt. 50 lbs. (22.68kg), Item Number 810087. UPC 7 85921-07090 4. Distributed by: United Sugar Producers & Refiners, Minneapolis, MN 55439. 2. Crystal Sugar, Net...

   Reason: Potential Wheat Kernel contamination.

   FDA recall H-1392-2026, reported 2026-09-30, ongoing

7. Wwf Operating CompanyLouisville, COClass II

   So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. 16 oz paper tub with an attached paper lid. Sold as a single unit multi serving tub. UPC 744473 476138. Distributed by For So Delicious Dairy Free...

   Reason: Product may contain foreign material: small stones and other hard objects.

   FDA recall H-1394-2026, reported 2026-09-30, ongoing

8. Kwok Shing, Inc.San Francisco, CAClass III

   American Ginsengs. PRODUCT OF WISCONSIN. NET WT: 4 oz. NET WT. 8 oz.

   Reason: Potential contamination with pesticides.

   FDA recall H-1393-2026, reported 2026-09-30, ongoing

New in the Federal Register

Rules, proposed rules, and notices from the FDA and USDA that touch food, labels, and organic.

• Rule · Health and Human Services Department Medical Devices; Cardiovascular Devices; Classification of the Hyperoxia Monitoring Device Adjunct to Pulse Oximetry

  The Food and Drug Administration (FDA) is classifying the hyperoxia monitoring device adjunct to pulse oximetry into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the hyperoxia monitoring device adjunct to pulse oximetry. We are taking this action because we have determined that classifying...

• Rule · Health and Human Services Department Medical Devices; Exemptions From Premarket Notification: Class II Devices; Certain Clinical Toxicology Test Systems

  The Food and Drug Administration (FDA) is publishing an order setting forth its final determination to exempt certain class II clinical toxicology test systems from premarket notification (510(k)) requirements, subject to certain limitations. This exemption from 510(k) requirements, subject to certain limitations, is immediately in effect for such devices. This exemption will decrease regulatory burdens on the...

• Rule · Health and Human Services Department Medical Devices; General and Plastic Surgery Devices; Classification of the Focused Ultrasound System for Non-Thermal, Mechanical Tissue Ablation

  The Food and Drug Administration (FDA) is classifying the focused ultrasound system for non-thermal, mechanical tissue ablation into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the focused ultrasound system for non-thermal, mechanical tissue ablation. We are taking this action because we...

• Rule · Health and Human Services Department Medical Devices; Immunology and Microbiology Devices; Classification of the High Throughput DNA Sequencing for Hereditary Cancer Predisposition Assessment Test System

  The Food and Drug Administration (FDA) is classifying the high throughput DNA sequencing for hereditary cancer predisposition assessment test system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the high throughput DNA sequencing for hereditary cancer predisposition assessment test...

• Notice · Health and Human Services Department Design and Safety Considerations for Clinical Trials Involving Ibogaine Drug Products; Request for Information

  The Food and Drug Administration (FDA or the Agency) is describing the approaches it is considering for the design of early- phase clinical trials of ibogaine drug products and is opening a public docket to receive comments. The Department of Health and Human Services (HHS) is funding clinical development of ibogaine, and the first federally supported trials are expected to study ibogaine in adults with opioid use...

• Notice · Health and Human Services Department Determination PRALIDOXIME CHLORIDE (Autoinjector) (Pralidoxime Chloride) Solution, 600 Milligrams/2 Milliliters (300 Milligrams/Milliliter), Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness

  The Food and Drug Administration (FDA, Agency, or we) has determined that PRALIDOXIME CHLORIDE (AUTOINJECTOR) (pralidoxime chloride) solution, 600 milligrams (mg)/2 milliliters (mL) (300 mg/mL), was not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to approve abbreviated new drug applications (ANDAs) for pralidoxime chloride solution, 600 mg/2 mL (300 mg/mL), if all...

• Notice · Health and Human Services Department Issuance of Priority Review Voucher; Rare Pediatric Disease Product; FAYUVI (rebisufligene etisparvovec-hopf)

  The Food and Drug Administration (FDA) is announcing the issuance of a priority review voucher to the sponsor of a rare pediatric disease product application. The Federal Food, Drug, and Cosmetic Act (FD&C Act) authorizes FDA to award priority review vouchers to sponsors of approved rare pediatric disease product applications that meet certain criteria. FDA is required to publish notice of the award of the priority...

• Notice · Health and Human Services Department Teva Pharmaceuticals USA, Inc., et al.; Withdrawal of Approval of 15 Abbreviated New Drug Applications; Correction

  The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register on May 7, 2026. The document announced the withdrawal of approval of 15 abbreviated new drug applications (ANDAs) from multiple applicants, withdrawn as of June 8, 2026. The document indicated that FDA was withdrawing approval of ANDA 210285 for dimethyl fumarate delayed-release capsule, 120 milligrams (mg) and 240...

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