FoodJan 21, 2026
Mangalm Tops Strawberry Jam INGREDIENTS: Sugar, Strawberry Pulp 30% recall — FDA H-0386-2026
Unapproved color (carmoisine).
Class IIFDA: OngoingMangalm LLC
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026146 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026334 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026180 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026211 records · 4 categories
2026 recalls — page 96
Records are ordered by the best available source date.
FoodJan 21, 2026
Ukrop's 6" Pound Cake with Buttercream Icing/Red Roses NET WT recall — FDA H-0397-2026
Undeclared Soy. Label did not include soy, which was used in product.
Class IIFDA: OngoingUkrop's Homestyle Foods, LLC
FoodJan 21, 2026
Ukrop's 6" Pound Cake with Buttercream Icing/Pink Roses NET WT recall — FDA H-0396-2026
Undeclared Soy. Label did not include soy, which was used in product.
Class IIFDA: OngoingUkrop's Homestyle Foods, LLC
FoodJan 21, 2026
Mangalm Tops Mixed Fruit Jam INGREDIENTS: Sugar, Mixed Fruit Pulp 48% recall — FDA H-0387-2026
Unapproved color (carmoisine).
Class IIFDA: OngoingMangalm LLC
FoodJan 21, 2026
GUSTO GROUP DPA161 Shrimp Paste recall — FDA H-0390-2026
Product tested high for lead.
Class IIFDA: TerminatedGUSTO GROUP, INC.
FoodJan 21, 2026
Herbs Forever HerbsForever- Gastro Care recall — FDA H-0404-2026
Potential undeclared allergen ingredient (Wheat)
Class IFDA: TerminatedHerbs Forever
FoodJan 21, 2026
Fran's Chocolates Fran s PureBar Almondmilk Chocolate 46% Madagascar recall — FDA H-0399-2026
undeclared hazelnut.
Class IFDA: TerminatedFran's Chocolates Ltd
FoodJan 21, 2026
Ukrop's 6" Pound Cake with Buttercream Icing/Confetti NET WT recall — FDA H-0395-2026
Undeclared Soy. Label did not include soy, which was used in product.
Class IIFDA: OngoingUkrop's Homestyle Foods, LLC
FoodJan 21, 2026
GUSTO GROUP Shrimp Paste recall — FDA H-0389-2026
Product tested high for lead.
Class IIFDA: TerminatedGUSTO GROUP, INC.
DrugJan 21, 2026
Clindamycin Phosphate USP, 1% (10 mg/mL), Topical Solution, 60 mL per applicator bottle recall — FDA D-0257-2026
Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay.
Class IIIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC
DrugJan 21, 2026
GOLD STAR DISTRIBUTION Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC recall — FDA D-0263-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
DrugJan 21, 2026
Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets recall — FDA D-0259-2026
Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.
Class IIFDA: OngoingAlvogen, Inc
DrugJan 21, 2026
Advanced Pharmaceutical Technology TESTO-100 CIII (testosterone 100 mg), 10 Sterile Pellets recall — FDA D-0258-2026
Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.
Class IIFDA: OngoingAdvanced Pharmaceutical Technology, Inc.
DrugJan 21, 2026
GOLD STAR DISTRIBUTION Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box recall — FDA D-0261-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
DrugJan 21, 2026
GOLD STAR DISTRIBUTION Halls Cough Drops a) BAGS, MENTHOL, 12CT recall — FDA D-0278-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
DrugJan 21, 2026
GOLD STAR DISTRIBUTION Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC recall — FDA D-0286-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
DrugJan 21, 2026
GOLD STAR DISTRIBUTION Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct recall — FDA D-0287-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
DrugJan 21, 2026
GOLD STAR DISTRIBUTION TUMS a) Assorted, 12 Ct recall — FDA D-0279-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
DrugJan 21, 2026
GOLD STAR DISTRIBUTION Petroleum jelly: a) Vaseline Petroleum Jelly, 1.75, 12CT, UPC recall — FDA D-0285-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
DrugJan 21, 2026
GOLD STAR DISTRIBUTION TYLENOL a) 500 MG., 2'S DISPLAY, 50CT recall — FDA D-0277-2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
VehicleJan 15, 2026
Ford engine block heater recall — NHTSA campaign 26V012000
Ford Motor Company (Ford) is recalling certain 2016-2018 Focus, 2019 Explorer, and 2024 Explorer vehicles. The engine block heater may crack and develop a coolant leak, causing it to short…
engine block heaterFord Motor Company
VehicleJan 15, 2026
Ford engine block heater recall — NHTSA campaign 26V011000
Ford Motor Company (Ford) is recalling certain 2013-2018 Focus, 2013-2019 Escape, and 2015-2016 MKC vehicles equipped with a 2.0L engine. The engine block heater may crack and develop a…
engine block heaterFord Motor Company
Medical DeviceJan 14, 2026
Securitas Healthcare Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware recall — FDA Z-1031-2026
Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert…
Class IIFDA: OngoingSecuritas Healthcare LLC
Medical DeviceJan 14, 2026
Integra LifeSciences Codman CereLink ICP Sensor Basic Kit recall — FDA Z-1037-2026
Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
Class IIFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
About the 2026 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.