The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

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2651–2675 of 30649

  • HighFDA (Drugs)·D-0267-2026·2026-01-21

    DayQuil Cold & Flu Recalled for Insanitary Manufacturing Conditions

    Gold Star Distribution is recalling DayQuil Cold & Flu 32CT/2PK packages nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The distribution center was found to have insanitary conditions including rodent exposure and activity.

    Product
    DAYQUIL COLD & FLU, 32CT/2PK
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0263-2026·2026-01-21

    FDA Recalls Alka-Seltzer Products for Sanitation Violations in Distribution Center

    Gold Star Distribution Inc. is recalling Alka-Seltzer Original and Plus Cold & Flu products distributed nationwide due to insanitary conditions and documented rodent activity in their distribution facility.

    Product
    Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0264-2026·2026-01-21

    Benadryl 25'S 2PK Recalled Due to Distribution Center Insanitary Conditions

    Benadryl 25'S 2PK boxes are being recalled nationwide due to insanitary conditions and rodent exposure in the distribution center. Affected consumers should stop using these products.

    Product
    Benadryl, 25'S 2PK Box, UPC 815556020316
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1078-2026·2026-01-21

    MOSAIQ Oncology System Software Defect May Cause Treatment Overdelivery

    Elekta's MOSAIQ oncology system may deliver cancer treatment twice due to a software error in specific workflow scenarios involving partial treatments.

    Product
    MOSAIQ Oncology Information System with Particle Therapy License (License Kit 45700000000IQRO)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1017-2026·2026-01-21

    Canon MRI Machines Risk Helium Vessel Rupture From Ice Formation

    Canon's VANTAGE GALAN 3T MRI machines may accumulate ice in the magnet vent system, preventing helium gas escape and potentially rupturing the helium vessel, causing gas release into the scanning room.

    Product
    VANTAGE GALAN 3T Model MRT-3020/MEXL-3020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1090-2026·2026-01-21

    Medline Stryker robotics urology kits recalled for irrigation fluid leakage risk

    Medline is recalling robotics urology procedure kits with Stryker Strykeflow 2 Suction Irrigators due to a 2024 design change that allows irrigation solution to leak and emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1096-2026·2026-01-21

    da Vinci SP Access Port Kit System Tray Cracks Risk Sterility Breach

    Intuitive Surgical is recalling da Vinci SP Access Port Kits because the system tray may develop cracks that could breach sterility during surgical use.

    Product
    da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1054-2026·2026-01-21

    Medline IV Administration Kits Recalled for Stuck Check Valve Components

    Medline kits containing B. Braun IV Administration Sets are recalled because check valve components may become stuck, potentially affecting medication delivery. Lot Number 25HBQ850 is affected.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL PACK, Medline kit SKU DYNJ54488A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1084-2026·2026-01-21

    Asserachrom HPIA Diagnostic Test Kit Recalled Due to Potential Defect

    Diagnostica Stago is recalling Asserachrom HPIA diagnostic test kits (lot 271288) due to a potential defect that may produce negative test results. The kits detect antibodies associated with heparin-induced thrombocytopenia.

    Product
    Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (PF4) antibodies generated during the type II heparin-induced thrombocytopenia (HIT type II) by ELISA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1093-2026·2026-01-21

    ThinPrep CytoLyt Solution Recalled for Fungal Contamination

    Hologic has recalled ThinPrep CytoLyt Solution due to fungal contamination detected in one lot. The buffered cell wash solution may cause infection if used in diagnostic procedures.

    Product
    ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1058-2026·2026-01-21

    Medline IV Administration Sets Recalled Due to Stuck Check Valve Risk

    Medline has recalled approximately 1,725 IV Administration Sets containing B. Braun components because check valves may become stuck in open or closed positions, potentially preventing medication delivery or allowing uncontrolled fluid flow.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) ADMIN KIT, Medline kit SKU DYKS1339B; 2) ADMIN KIT, Medline kit SKU DYKS1339C; 3) QCASC WELCOME KIT, Medline kit SKU DYKS1359B; 4) ADMISSION KIT, Medline kit SKU DYKS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1088-2026·2026-01-21

    Medline Surgical Procedure Kits Recalled Due to Irrigation Solution Leakage

    Medline is recalling 12,584 surgical procedure kits containing Stryker Strykeflow 2 irrigators due to a design defect that causes irrigation solution to leak and emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0285-2026·2026-01-21

    Petroleum Jelly Products Recalled for Rodent Contamination Risk

    Gold Star Distribution is recalling multiple petroleum jelly products distributed nationwide due to insanitary conditions including rodent exposure discovered in their distribution center.

    Product
    Petroleum jelly: a) Vaseline Petroleum Jelly, 1.75, 12CT, UPC: 6001085120946; b) Vaseline Men Cooling Petroleum Jelly, 100ML, 12CT, UPC: 60022141; c) Vaseline Vitamin E, Petroleum Jelly, 100ML, 12CT, UPC: 6001085121028; MEN FRESH PETROLEUM JELLY, 100ML, 12CT, UPC: 60022127; d) Lu
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0279-2026·2026-01-21

    TUMS Antacid Tablets Recalled Due to Insanitary Conditions in Distribution Center

    TUMS antacids manufactured by Gold Star Distribution Inc are being recalled due to insanitary conditions including rodent exposure in the distribution center. No illnesses have been reported.

    Product
    TUMS a) Assorted, 12 Ct.; b) Extra Strength (EX) Assorted Berries, 12-count #1194A *05/27; c)Extra Strength (EX) Assorted Fruit, 12-count, #1194C *03/27
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0271-2026·2026-01-21

    Motrin Pain Reliever Recalled for Distribution Center Sanitation Violations

    Gold Star Distribution Inc. recalls all lots of Motrin 2's pain reliever (50-count dispensers) distributed nationwide due to CGMP deviations including insanitary conditions and rodent exposure at their distribution center.

    Product
    MOTRIN 2'S DISP.- 50CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0287-2026·2026-01-21

    Colgate and Crest toothpaste recalled due to rodent exposure in distribution center

    Multiple Colgate and Crest toothpaste products distributed nationwide are being recalled due to insanitary conditions and rodent exposure at Gold Star Distribution Inc's distribution center.

    Product
    Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct; UPC: 035000511065; b) COLGATE, TOOTHPASTE, Regular, 2.5oz, 24ct, UPC: 035000511058; c) COLGATE, TOOTHPASTE, TRIPLE, 2.5oz, 24ct, UPC: 035000512109; d) COLGATE, TOOTHPASTE, MINT ZING, 24CT, 2.5oz, UPC: 035000744609; COLGA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0286-2026·2026-01-21

    Multiple Deodorant and Body Spray Products Recalled for Contamination Risk

    Gold Star Distribution is recalling multiple deodorant and body spray products due to insanitary conditions and rodent exposure at their distribution center. Affected brands include Axe, Lucky, and Lady deodorants distributed nationwide.

    Product
    Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC: 600108736469; b) LUCKY MENS STICK DEODORANT, SPRING FRESH, 24CT, 2.5 OZ, UPC: 808829111668; c) LUCKY MENS STICK DEODORANT, FRESH COMFORT, 24CT, 1.6 OZ, UPC: 808829089103; d) LADY DEODORANT, CHERRY BLOSSOSM, 24CT, 1.8oz,
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0282-2026·2026-01-21

    Carmex Lip Balm Recalled for Insanitary Conditions at Distribution Center

    Gold Star Distribution Inc. is recalling Carmex lip balm products distributed nationwide due to insanitary conditions, including rodent exposure and activity, found at their distribution center during a CGMP inspection.

    Product
    Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0261-2026·2026-01-21

    Advil Ibuprofen Dispenser Packs Recalled for Rodent Contamination Risk

    Gold Star Distribution Inc. is recalling Advil Ibuprofen and PM dispenser packs distributed nationwide due to insanitary conditions and rodent exposure in the distribution center.

    Product
    Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0278-2026·2026-01-21

    Halls Cough Drops Recalled Due to Distribution Center Sanitation Issues

    Gold Star Distribution Inc is recalling multiple varieties of Halls Cough Drops distributed nationwide due to insanitary conditions and rodent activity discovered in their distribution center.

    Product
    Halls Cough Drops a) BAGS, MENTHOL, 12CT; b) BAGS, HONEY LEM, 12CT; c) BAGS, DEFENSE CITRUS, 12CT; d) BAGS, CHERRY, 12CT; e) M. CHERRY, 20 STK; f) BRAZIL, Cherry, 21CT/27.5G; f) LEMON. HONEY, 20CT #1180E; g) LIME FRESH, 20CT, #1182; h) MENTHOL BLUE, 20CT, #1180A; i) BRAZIL, Menth
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1086-2026·2026-01-21

    Medline surgical kits recalled for leaking irrigation solution during procedures

    Medline medical procedure kits containing Stryker Strykeflow 2 suction irrigators are recalled. A 2024 design change causes irrigation solution to leak and vaporized saline to emit during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF, REF CDS860235L; 2) GENERAL LAPAROSCOPIC, REF CDS930223M; 3) LAP CHOLE CDS, REF CDS983678K; 4) LAPAROSCOPY PELV CDS, REF CDS983679K; 5) LAP CHOLE CDS-LF, REF CDS983752M; 6) LAP CHOLE CDS-LF,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1045-2026·2026-01-21

    Nuclear Medicine Imaging Systems: Risk of Detector Fall During Transport

    GE HealthCare is recalling certain nuclear medicine imaging systems with potentially compromised detector mounting mechanisms that could fail during transport. No injuries have been reported, but detector falls could cause serious harm.

    Product
    SMV DSI, System, Tomography, Computed, Emission
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1041-2026·2026-01-21

    AIRO CT Pendant Upgrade Missing Safe Hand Position Warning Label

    Mobius Imaging is recalling 26 AIRO CT pendant upgrade components lacking a required 'Safe Hand Position Warning' label. The missing label could prevent users from recognizing safe hand positioning during equipment operation.

    Product
    Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1049-2026·2026-01-21

    Medline IV Administration Kits Recalled for Check Valve Sticking Risk

    Medline is recalling IV administration kits containing B. Braun components due to check valve defects that may become stuck. The kits were distributed nationwide and used in anesthesia procedures.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B
    Category
    Medical Device
    Distribution
    Distributed nationwide