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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2201–2225 of 30649

  • HighFDA (Drugs)·D-0327-2026·2026-02-18

    Testosterone and Anastrozole Pellets Recalled for Potential Metal Contamination

    Asteria Health recalled Testosterone-Anastrozole injectable pellets due to potential metal particulate contamination. Affected lots 254000107 and 254000111 were distributed nationwide.

    Product
    Testosterone 75mg, Anastrozole 4mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4079-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0319-2026·2026-02-18

    Testosterone Pellets Recalled Due to Potential Metal Contamination

    F.H. INVESTMENTS, Inc. (dba Asteria Health) is recalling testosterone pellets nationwide due to potential metal particulate matter contamination. Approximately 60,868 pellets across five lot numbers are affected.

    Product
    Testosterone, 37.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1037-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1359-2026·2026-02-18

    Surepulse VS Cap Large Medical Device Recalled for Incorrect Sizing Guide

    Surepulse Medical is recalling the VS Cap Large, a component of the VS Newborn Heart Rate Monitor, due to incorrect sizing information in the labeling.

    Product
    Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0497-2026·2026-02-18

    Sugar substitute packets recalled due to undeclared aspartame ingredient

    Domino Foods is recalling Sodexo Stars Saccharin packets because the product contains undeclared aspartame. The recall affects 2,023 cases distributed across multiple states.

    Product
    Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West Palm Beach, FL 33041
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1329-2026·2026-02-18

    Medline medical convenience kits recalled for open seals on applicators

    Medline Industries is recalling 7,570 medical convenience kits containing BD ChloraPrep Triple Swabsticks due to potentially open seals on applicator packaging. The kits are distributed nationwide to hospital and clinical settings.

    Product
    Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710; 2) LINE KIT, Kit SKU DYNDA1857A; 3) PICC REMOVAL KIT, Kit SKU DYNDC1978A; 4) PORT ACCESS TRAY, Kit SKU DYNDC2367; 5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B; 6) CVC DRESSING
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1332-2026·2026-02-18

    Medline Suture Removal Trays Recalled Due to Potentially Open Packaging Seals

    Medline Industries is recalling 2,448 suture removal kits due to potentially open packaging seals on BD ChloraPrep Triple Swabsticks applicators, which could compromise sterility.

    Product
    Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0338-2026·2026-02-18

    Oxycodone Hydrochloride Tablets Recalled for Defective Blister Seals

    Amerisource Health Services is recalling Oxycodone Hydrochloride Tablets, 5 mg, nationwide due to defective blister card seals. Weak or non-existent seals may allow tablets to fall out of their cavities.

    Product
    OXYCODONE HYDROCHLORIDE — OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0302-2026·2026-02-18

    Pro Numb Tattoo Numbing Spray Recalled for Manufacturing Deviations

    Pro Numb Tattoo Numbing Spray (5% Lidocaine) is being recalled nationwide due to manufacturing process violations (cGMP deviations). Affected lots are J01-J14 and J55-J69 in 1 oz and 4 oz bottles.

    Product
    PRO NUMB — PRO NUMB (TATTOO NUMBING SPRAY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0303-2026·2026-02-18

    Pro Numb tattoo numbing spray recalled for manufacturing standard violations

    Pro Numb Tattoo Numbing Spray (lot J15) is recalled nationwide due to manufacturing process deviations. The voluntary recall was initiated February 2, 2026.

    Product
    PRO NUMB SENSITIVE SKIN — PRO NUMB SENSITIVE SKIN (NUMBING SPRAY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0306-2026·2026-02-18

    Tablets of Doxazosin Mesylate 4 mg Recalled for Incorrect Imprinting

    Unichem Pharmaceuticals is recalling 60,000 Doxazosin Mesylate 4 mg tablets due to incorrect imprinting. Patients should check their medication bottles and contact their pharmacy if they have Lot #GDSH25006.

    Product
    DOXAZOSIN MESYLATE — DOXAZOSIN MESYLATE (DOXAZOSIN MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1357-2026·2026-02-18

    Newborn Heart Rate Monitor Cap Has Incorrect Sizing Labeling

    Surepulse Medical recalls VS Cap Small components of newborn heart rate monitors due to incorrect sizing guidance in the labeling. The labeling error could affect proper device fit.

    Product
    Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1360-2026·2026-02-18

    Surepulse VS Cap Extra Large Recalled for Incorrect Sizing Guide

    The Surepulse VS Cap Extra Large component of newborn heart rate monitors has been recalled because the product labeling contains an incorrect sizing guide.

    Product
    Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1337-2026·2026-02-18

    Straumann Impression Post Closed Tray Recalled for Color Mismatch in Packaging

    Straumann USA is recalling 561 units of WB Impression Post Closed Tray due to incorrect impression caps in packaging. The caps are magenta instead of the intended brown color.

    Product
    WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1358-2026·2026-02-18

    FDA Recalls Surepulse Newborn Heart Rate Monitor Cap for Labeling Error

    Surepulse Medical is recalling certain newborn heart rate monitor caps due to incorrect sizing information in the labeling. The issue affects specific lot numbers distributed in the US and internationally.

    Product
    Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1356-2026·2026-02-18

    Surepulse Newborn Heart Rate Monitor Cap Recalled for Incorrect Sizing Label

    Surepulse Medical recalled the VS Cap Extra Small component of its newborn heart rate monitor due to an incorrect sizing guide in the product labeling.

    Product
    Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26268·2026-02-12

    Watkins Manufacturing Recalls Highlife Collection Spa Jets Due to Drowning Hazard

    Watkins Manufacturing is recalling Hydromassage rotary jets in Highlife Collection spas because they can create suction that entangles user hair and submerges the head, posing a drowning hazard. About 32,900 units are affected.

    Product
    Hydromassage Rotary Jet (6 fin) in Highlife Collection spas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26261·2026-02-12

    SOOWERY 6-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards

    SOOWERY 6-drawer dressers pose tip-over and entrapment hazards to children unless anchored to the wall. The dressers violate mandatory STURDY Act safety standards.

    Product
    SOOWERY 6-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26266·2026-02-12

    CheerKid Baby Bath Seats Recalled Due to Risk of Drowning from Tipping

    CheerKid Baby Bath Seats have been recalled because they are unstable and can tip over while in use, posing a serious drowning risk. About 590 units were sold on Amazon in September 2025.

    Product
    CheerKid Baby Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26267·2026-02-12

    Beloems Adult Portable Bed Rails Recalled for Entrapment and Fall Hazards

    Beloems Adult Portable Bed Rails sold on Amazon from June-October 2025 are recalled for serious entrapment and fall hazards. The bed rails violate mandatory standards and pose risks of asphyxiation, falls, and lacerations.

    Product
    Beloems Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26260·2026-02-12

    3-Pack Smoke Detectors Recalled for Failure to Alarm During Fire

    LShome 3-Pack Smoke Detectors have been recalled because their sensor thresholds are set too high, preventing timely alarm response during fires. Consumers should stop use immediately and contact the distributor for refund instructions.

    Product
    3-Pack Smoke Detector Fire Alarms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26265·2026-02-12

    Colombia-themed Magnetic Board Games Recalled for Magnet Ingestion Hazard to Children

    Surveying Accessories Cheaper recalls Colombia-themed magnetic board games sold via Amazon and Centro Envíos Aventura because loose game pieces contain high-powered magnets that pose an ingestion hazard to children, potentially causing intestinal blockage, perforation, or death.

    Product
    Colombia-themed Magnetic Board Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0454-2026·2026-02-11

    Everpress Juice Spicy Lemonade Recalled for Potential Bacterial Contamination

    Everpress Juice is recalling JUICE from the Raw spicy lemonade products due to potential pathogenic bacteria from under-processing. The product was distributed in multiple states across the United States.

    Product
    JUICE from the Raw, spicy lemonade
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Drugs)·D-0304-2026·2026-02-11

    Green Lumber Natural Fuel For Men Capsules Recalled as Unapproved Drug

    Green Lumber Natural Fuel For Men capsules are recalled because FDA determined the product was marketed without required approval and contains the active ingredient tadalafil.

    Product
    Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660
    Category
    Drug
    Distribution
    Distributed nationwide