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
Latest records
Latest recalls — page 117
The newest recall records with useful source details are listed here.
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.
Medical DeviceJan 14, 2026
HFD100 Head Fixation Device HFD100 recall — FDA Z-1034-2026
Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays, requirement for alternate head…
Class IIFDA: OngoingIMRIS Imaging Inc.
Medical DeviceJan 14, 2026
Beckman Coulter UniCel Dxl 800, Part numbers: 973100, A71456, A71457, A25288 recall — FDA Z-1026-2026
Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceJan 14, 2026
Beckman Coulter UniCel Dxl 600, Part numbers: A71460, A71461, A30260 recall — FDA Z-1025-2026
Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceJan 14, 2026
Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS recall — FDA Z-1035-2026
Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient may experience shortness of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJan 14, 2026
CareFusion 303 BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 recall — FDA Z-1028-2026
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJan 14, 2026
Integra LifeSciences Codman Microsensor Basic Kit recall — FDA Z-1036-2026
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
Vision RT The AlignRT InBore system contains six Class 1 lasers which enables the system s recall — FDA Z-0998-2026
Vision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was omitted…
Class IIFDA: OngoingVision RT Ltd
FoodJan 14, 2026
Ambriola Co., Inc., The Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & recall — FDA H-0374-2026
Product tested positive for Listeria Monocytogenes.
Class IFDA: CompletedAmbriola Co., Inc., The
FoodJan 14, 2026
Rovira Biscuit 3 recall — FDA H-0363-2026
Undeclared colors FD&C Yellow #6, and FD&C Red 40
Class IIFDA: TerminatedRovira Biscuit Corporation
FoodJan 14, 2026
Rovira Biscuit Vainilla Crackers, Great Value recall — FDA H-0362-2026
Undeclared colors FD&C Yellow #6, and FD&C Red 40
Class IIFDA: TerminatedRovira Biscuit Corporation
FoodJan 14, 2026
Ambriola Co., Inc., The Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & recall — FDA H-0367-2026
Product tested positive for Listeria Monocytogenes.
Class IFDA: CompletedAmbriola Co., Inc., The
FoodJan 14, 2026
Fresh & Ready Foods Eggs Potatoes Cheese Tacos, Evergreen Refreshments brand recall — FDA H-0356-2026
Foreign material.
Class IIFDA: TerminatedFresh & Ready Foods LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026300 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories