FoodOct 15, 2025
Toto S'Mores Ooey Gooey Cookie recall — FDA H-0071-2026
Product label contains conflicting statements about inclusion and being free of Soy ingredient.
Class IIFDA: TerminatedToto Foods, Inc.
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 43
Records are ordered by the best available source date.
FoodOct 15, 2025
Harris Teeter NET WT 5.0oz recall — FDA H-0030-2026
Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefore the allergen milk was not listed in…
Class IFDA: TerminatedHarris Teeter
FoodOct 15, 2025
M.O.M Enterprises, LLC Organic BABY bedtime drops recall — FDA H-0025-2026
Potential yeast contamination.
Class IIFDA: OngoingM.O.M Enterprises, LLC.
FoodOct 15, 2025
Edens Elixirs Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet recall — FDA H-0131-2026
Undeclared Yellow #5
Class IIFDA: TerminatedEdens Elixirs, LLC
FoodOct 15, 2025
Gansu Zhaofeng Agricultural Development Co G&L Food Dried Bean Curd Net WT 17.6 OZ recall — FDA H-0111-2026
Undeclared allergen (wheat).
Class IIIFDA: OngoingGansu Zhaofeng Agricultural Development Co., Ltd.
FoodOct 15, 2025
Edens Elixirs Eskay Brands Mint flavored tablets recall — FDA H-0130-2026
Undeclared Yellow #5
Class IIFDA: TerminatedEdens Elixirs, LLC
FoodOct 15, 2025
Organicare Nature's Science FemiClear Daily Bladder Strength Dietary Supplement, 28 Count recall — FDA H-0031-2026
Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303.
Class IIFDA: TerminatedOrganicare Nature's Science, LLC
FoodOct 15, 2025
Western United Fish Company Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193 recall — FDA H-0023-2026
Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi…
Class IFDA: TerminatedWestern United Fish Company Inc
FoodOct 15, 2025
Harris Teeter NET WT 5.0OZ recall — FDA H-0029-2026
Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefore the allergen milk was not listed in…
Class IFDA: TerminatedHarris Teeter
FoodOct 15, 2025
Country Eggs o Nagatoshi Large AA Brown Omega-3 1 dozen cartons o Nijiya recall — FDA H-0011-2026
Shell egg product potentially contaminated with salmonella.
Class IFDA: TerminatedCountry Eggs, LLC
DrugOct 15, 2025
GenoGenix BPC-157/Thymosin Beta-4 for Injection, a) 10/10mg, b) 15/15mg, c) 15mg/15mg, all recall — FDA D-0086-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingGenoGenix LLC
DrugOct 15, 2025
Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose recall — FDA D-0008-2026
Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.
Class IIFDA: OngoingDr. Reddy's Laboratories, Inc.
DrugOct 15, 2025
Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 90 Tablets per bottle recall — FDA D-0006-2026
Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.
Class IIFDA: OngoingACCORD HEALTHCARE, INC.
DrugOct 15, 2025
Acuity Specialty Products Wyandotte, Sanifect E3, Hand Sanitizer recall — FDA D-0004-2026
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk…
Class IIFDA: OngoingAcuity Specialty Products, Inc.
DrugOct 15, 2025
GenoGenix Elite Stack MSC Exosome Reconstitution Solution for Injection, all strengths and recall — FDA D-0074-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingGenoGenix LLC
DrugOct 15, 2025
Acuity Specialty Products AFCO, Hand Sanitizer recall — FDA D-0005-2026
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk…
Class IIFDA: OngoingAcuity Specialty Products, Inc.
DrugOct 15, 2025
The Harvard Drug Group LLC dba Major Major ChlorproMAZINE Hydrochloride Tablets, USP, 200 recall — FDA D-0013-2026
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Class IIFDA: OngoingThe Harvard Drug Group LLC dba Major Pharmaceuticals…
DrugOct 15, 2025
Norgestimate and Ethinyl Estradiol Tablets, USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and recall — FDA D-0007-2026
Failed Content Uniformity Specifications
Class IIFDA: OngoingAvKARE
DrugOct 15, 2025
GenoGenix Reconstitution XO Solution for Injection, all strengths and presentations recall — FDA D-0081-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingGenoGenix LLC
VehicleOct 13, 2025
Ford camera recall — NHTSA campaign 25V695000
Ford Motor Company (Ford) is recalling certain 2015-2019 Flex, 2015 Explorer, Lincoln MKT, Lincoln MKZ, 2015-2016 C-Max, Escape, Taurus, 2016 Fusion, 2018-2019 Taurus, 2019 Lincoln MKT,…
cameraFord Motor Company
VehicleOct 10, 2025
Ford windshield recall — NHTSA campaign 25V683000
Ford Motor Company (Ford) is recalling certain 2025 Bronco and Ranger vehicles. During manufacturing, the windshield may not have been properly bonded to the vehicle, allowing it to detach…
windshieldFord Motor Company
VehicleOct 10, 2025
Escape pads recall — NHTSA campaign 25V693000
Ford Motor Company (Ford) is recalling certain 2020 Escape vehicles. The rear brake pads may have been manufactured incorrectly, which can reduce brake function in the event of a brake…
padsFord Motor Company
VehicleOct 10, 2025
Mustang body control module/bcm recall — NHTSA campaign 25V689000
Ford Motor Company (Ford) is recalling certain 2021-2023 Mustang vehicles repaired incorrectly under recall number 23V727. The brake fluid level sensor may not activate the visual warning…
body control module/bcmFord Motor Company
VehicleOct 10, 2025
Ford engine block heater recall — NHTSA campaign 25V685000
Ford Motor Company (Ford) is recalling certain 2016-2019 Lincoln MKC, 2016-2023 Explorer, 2019-2020 Fusion, 2019-2024 Ranger, 2020-2022 Lincoln Corsair, Escape, 2021-2024 Bronco, Bronco…
engine block heaterFord Motor Company
About the 2025 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.