FoodSep 24, 2025
Hi-Tech Pharmaceuticals FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS recall — FDA H-0586-2025
Unapproved Drug Claims.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
September 2025 recalls — page 3
These records include useful source details for the selected month.
FoodSep 24, 2025
Fresh & Ready Foods Spanish Club Ciabatta recall — FDA H-0612-2025
undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
Class IFDA: TerminatedFresh & Ready Foods LLC
FoodSep 24, 2025
HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & recall — FDA H-0592-2025
Unapproved Drug Claims and Misbranded.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
FoodSep 24, 2025
Cheesecake Royale Bake-a-holic Pecan Bars Cheesecake Royale Pecan Bars recall — FDA H-0602-2025
Review of Label determined allergen was listed as unsalted butter/ heavy cream. In one instance of identified label, there was no milk or dairy listed listed in Contains statement. Further…
Class IIFDA: TerminatedCheesecake Royale, Inc.
FoodSep 24, 2025
BulkSupplements.com Generic name: Inositol recall — FDA H-0619-2025
Finished product possibly contaminated with pathogenic Staphylococcus aureus.
Class IIFDA: TerminatedHARD EIGHT NUTRITION LLC
FoodSep 24, 2025
Hi-Tech Pharmaceuticals Top Secret Nutrition extra strength uric control fast acting recall — FDA H-0599-2025
Unapproved Drug Claims.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
FoodSep 24, 2025
NEUHAUS brand ORIGINAL BELGIAN CHOCOLATE recall — FDA H-0582-2025
Product contains undeclared wheat.
Class IFDA: TerminatedNeuhaus nv
FoodSep 24, 2025
Admiralty Island Fisheries Inc dba AquaStar AquaStar Cocktail Shrimp, 4oz recall — FDA H-0583-2025
Product may be contaminated with Cesium-137 (Cs-137).
Class IIFDA: OngoingAdmiralty Island Fisheries Inc dba AquaStar (USA) Corp.
FoodSep 24, 2025
Admiralty Island Fisheries Inc dba AquaStar Frozen Mercado Kroger Cooked Shrimp - Medium recall — FDA H-0584-2025
Product may be contaminated with Cesium-137 (Cs-137).
Class IIFDA: OngoingAdmiralty Island Fisheries Inc dba AquaStar (USA) Corp.
FoodSep 24, 2025
HI-TECH PHARMACEUTICALS FISH OIL HEART AND BRAIN HEALTH recall — FDA H-0589-2025
Unapproved Drug Claims.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
FoodSep 24, 2025
Southwind Foods LLC dba Great American Seafood Best Yet recall — FDA H-0604-2025
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Class IIFDA: TerminatedSouthwind Foods LLC dba Great American Seafood Imports…
FoodSep 24, 2025
Endico brand MIXED VEGETABLES recall — FDA H-0617-2025
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedEndico Potatoes Inc
FoodSep 24, 2025
Fresh & Ready Foods Tuscan Artichoke and Mozzarella Salad recall — FDA H-0613-2025
undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
Class IFDA: TerminatedFresh & Ready Foods LLC
FoodSep 24, 2025
HI-TECH PHARMACEUTICALS BETA SITOSTEROL recall — FDA H-0588-2025
Unapproved Drug Claims and Misbranded.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
FoodSep 24, 2025
Admiralty Island Fisheries Inc dba AquaStar Frozen AquaStar Breaded Shrimp, Butterfly recall — FDA H-0585-2025
Product may be contaminated with Cesium-137 (Cs-137).
Class IIFDA: OngoingAdmiralty Island Fisheries Inc dba AquaStar (USA) Corp.
FoodSep 24, 2025
Wang Globalnet recall — FDA H-0611-2025
Oyster product potentially contaminated with Norovirus
Class IIFDA: TerminatedWang Globalnet
FoodSep 24, 2025
Hi-Tech Pharmaceuticals PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 recall — FDA H-0598-2025
Unapproved Drug Claims and Misbranded.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
DrugSep 24, 2025
Sulfamethoxazole and Trimethoprim Tablets, USP 800mg / 160mg Double Strength recall — FDA D-0654-2025
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a…
Class IIFDA: OngoingNorthwind Pharmaceuticals LLC
DrugSep 24, 2025
Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL), Hazardous Drug recall — FDA D-0651-2025
cGMP deviations: Temperature excursion during transportation.
Class IIFDA: OngoingSandoz Inc
DrugSep 24, 2025
Cyclobenzaprine Hydrochloride Tablets, USP, 10 mg, 90-count bottle recall — FDA D-0655-2025
Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in…
Class IFDA: OngoingUnichem Pharmaceuticals USA Inc.
DrugSep 24, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, packaged as a) 50 (5x10) blisterpacks recall — FDA D-0647-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No…
Class IIFDA: OngoingAmerisource Health Services LLC
DrugSep 24, 2025
KIT FOR THE PREPARATION OF TECHNETIUM TC99M MERTIATIDE Kit for the Preparation of Technetium recall — FDA D-0658-2025
Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC
DrugSep 24, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 100 mg, 100 (10x10) blisterpack per carton recall — FDA D-0649-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No…
Class IIFDA: OngoingAmerisource Health Services LLC
DrugSep 24, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 (10x10) blisterpacks recall — FDA D-0648-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No…
Class IIFDA: OngoingAmerisource Health Services LLC
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.