FoodJan 21, 2026
Herbs Forever HerbsForever- Gastro Care recall — FDA H-0404-2026
Potential undeclared allergen ingredient (Wheat)
Class IFDA: TerminatedHerbs Forever
Latest records
Latest recalls — page 96
The newest recall records with useful source details are listed here.
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)
Medical DeviceJan 14, 2026
Securitas Healthcare Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware recall — FDA Z-1032-2026
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
Roche Diagnostics Operations The Elecsys Anti-TSHR immunoassay is a three-step competitive recall — FDA Z-1009-2026
Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or…
Class IIFDA: OngoingRoche Diagnostics Operations, Inc.
Medical DeviceJan 14, 2026
Siemens Medical Solutions USA LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model recall — FDA Z-0999-2026
A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceJan 14, 2026
Remote Diagnostic Technologies Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007 recall — FDA Z-1027-2026
Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If healthcare providers base…
Class IIFDA: OngoingRemote Diagnostic Technologies Ltd.
Medical DeviceJan 14, 2026
Meridian Bioscience Revogene C. difficile, in vitro diagnostic assay intended for use with recall — FDA Z-1019-2026
The affected lots show a decline in performance over time, which may lead to false-negative results.
Class IIFDA: OngoingMeridian Bioscience Inc.
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026332 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026210 records · 4 categoriesDecember 2025185 records · 4 categoriesNovember 202596 records · 3 categoriesOctober 2025139 records · 3 categoriesSeptember 2025116 records · 3 categories