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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626–650 of 26077

  • SevereFDA (Food)·H-0762-2026·2026-05-13

    Raw Cheddar Cheese Recalled for E. coli O157:H7 Multi-State Outbreak

    Raw Farm LLC is recalling raw cheddar cheese due to a multi-state outbreak of E. coli O157:H7. Affected consumers should not consume the product and should discard it or return it to the retailer.

    Product
    RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 835204001177 16 oz (4
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·H-0765-2026·2026-05-13

    Raw Cheddar Cheese Recalled Due to E. coli O157:H7 Outbreak

    Raw Farm shredded raw cheddar cheese is being recalled due to a multi-state E. coli O157:H7 outbreak. The product was distributed to consumers across multiple U.S. states.

    Product
    RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204000194
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·H-0692-2026·2026-05-13

    Chick-fil-A Milk Wash Recall Due to Potential Salmonella Contamination

    Griffith Foods is recalling nonfat dry milk (Milk Wash) sold to Chick-fil-A due to potential Salmonella contamination. The product was distributed across 15 states.

    Product
    MILK WASH NET WEIGHT: 50OZ (1417g) Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, GA 30349
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Devices)·Z-1981-2026·2026-05-13

    Angiographic Control Syringe Kits Recalled Due to Adapter Disconnection Risk

    American Contract Systems is recalling 7,311 convenience kits containing Medline angiographic control syringes. The rotating adaptor may unwind during use, potentially causing disconnection and risks including blood loss, infection, and air embolism.

    Product
    Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·H-0700-2026·2026-05-13

    Buttermilk Powder Recalled Due to Potential Salmonella Contamination

    California Dairies Inc. is recalling buttermilk powder due to potential Salmonella contamination. The affected product was distributed in the United States and to Mexico, Philippines, and Dominican Republic.

    Product
    Buttermilk Powder - paper bags 25 kg. (packed under 1 label: BMP Extra Grade Standard)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0766-2026·2026-05-13

    Raw Farm Cheddar Cheese Recalled for E. coli O157:H7 Outbreak

    Raw Farm Original Raw Cheddar (80 oz bulk) is being recalled due to a multi-state E. coli O157:H7 outbreak. Consumers should not consume this product and should discard or return it.

    Product
    RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2107-2026·2026-05-13

    Medline Neurosurgical Convenience Kits Sterilization Calibration Defect

    Medline is recalling 52 models of neurosurgical convenience kits due to calibration issues with sterilization equipment that may have compromised the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) NEURO SHUNT- CODMAN, Model Number: CDS860018G; 2) NEURO SHUNT- CODMAN, Model Number: CDS860018I; 3) KIT NEUR FUS LUM POST CRANDALL, Model Number: DYKMBNDL138; 4) KIT NEURO FUS LUM POST SANSUR, Model Number: DYKMBNDL142; 5) KIT NEURO FUS LUM P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2131-2026·2026-05-13

    BioCera Fibers Bioresorbable Bone Void Filler Recall

    Orthorebirth Co Ltd is recalling BioCera Fibers, a bioresorbable bone void filler, because the product falls outside standard specifications. The recall affects 1266 units distributed nationwide in California and Florida.

    Product
    BioCera Fibers, Bioresorbable Bone Void Filler, REF: ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2026·2026-05-13

    Medline Convenience Kits General Closure sterilization calibration issue

    Medline Industries is recalling Convenience Kits (Model DYKMBNDL200A) due to calibration issues in sterilization equipment that may have compromised sterility assurance. The kits were distributed nationwide.

    Product
    Medline Convenience Kits: 1) KIT GENERAL CLOSURE, Model Number: DYKMBNDL200A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2051-2026·2026-05-13

    Prodisc C SK cervical disc implant labeling mix-up recalled

    Centinel Spine is recalling Prodisc C SK U.S. Implant Extra Large cervical disc replacement devices due to a labeling mix-up where 6mm implants were labeled as 5mm and 5mm implants were labeled as 6mm.

    Product
    Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical disc replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2048-2026·2026-05-13

    LUX-DX II Arrhythmia Detector Monitoring Function Data Collection Issue

    Boston Scientific is recalling the LUX-DX II Model M302 and M312 arrhythmia detectors because some upgraded devices are not collecting PVC Burden data or monitoring for Bradyarrhythmia and Pause, with conflicting information shown in programming screens.

    Product
    LUX-DX II, Arrythmia detector and alarm, Model M302, with SERVER SW LATITUDE DRAGON US, Model 6460, Version 7.5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0721-2026·2026-05-13

    Loard's Butter Brickle Ice Cream recalled for undeclared allergens

    Loard's Butter Brickle Ice Cream (32 oz) recalled due to undeclared milk, almonds, and soy. Product distributed to Northern California ice cream parlors and grocery stores.

    Product
    Loard's Butter Brickle Ice Cream - 32 oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2065-2026·2026-05-13

    Physio-Control Defibrillators May Lack Required Performance Inspection

    Physio-Control defibrillators (LIFEPAK 15, 1000, 35, and 20e models) serviced between July 2023 and November 2025 may not have undergone required Performance Inspection Procedures, potentially preventing therapy delivery.

    Product
    LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958, 99577-001950, 99577-001962, 99577-002178, 99577-001372, 99577-00193
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2049-2026·2026-05-13

    LUX-Dx II Plus Arrythmia Detector Software Monitoring Feature Failure

    Boston Scientific's LUX-Dx II Plus implantable cardiac monitors may fail to collect PVC Burden data or monitor for abnormal heart rhythms in some upgraded devices, creating potential gaps in patient monitoring.

    Product
    LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUDE DRAGON EU (Europe), Model 6446, Version 7.5, or SERVER SW LATITUDE DRAGON AU (Australia/New Zealand), Model 6448, Version 7.5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2050-2026·2026-05-13

    Prodisc C SK Cervical Implant Size Labeling Mix-Up Recall

    Centinel Spine is recalling Prodisc C SK U.S. cervical disc implants due to a labeling mix-up: 6mm products were labeled as 5mm and 5mm products were labeled as 6mm, creating risk of implanting the wrong size.

    Product
    Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0761-2026·2026-05-13

    Target Deli Sesame Teriyaki Chicken Recalled for Undeclared Allergens

    Target Corporation is recalling Good & Gather Fresh from Our Deli Sesame Teriyaki Chicken with Rice (18 oz) due to undeclared sesame and soy allergens. The product was distributed across 21 states with use-by dates between April 15–27, 2026.

    Product
    Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. DPCI # 878-02-0227. UPC (01) 00250086000009 (3922) 00999. Distributed by SuperTarget Mpls, MN 55403.
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-2092-2026·2026-05-13

    Medline Convenience Kits sterilization and packaging calibration issues recalled

    Medline Industries is recalling multiple Convenience Kit models used in cardiac, vascular, and surgical procedures due to calibration issues with sterilization and packaging equipment that could impact sterility assurance. Approximately 39,341 units distributed worldwide may be affected.

    Product
    Medline Convenience Kits: 1) ANGIO PROCEDURE PACK, Model Number:00-401824AB; 2) OR ARTERIOGRAM, Model Number:CDS985094F; 3) INTRAVASOR CATH KIT, Model Number:DYK1060193I; 4) KIT SURG ONC LAP DIAG/CV CATH, Model Number:DYKMBNDL153; 5) KIT ACES INSERT PERCUTANEOUS T, Model
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2110-2026·2026-05-13

    Medline Convenience Kits for C-Section and Obstetric Procedures

    Medline Industries is recalling 12,529 units of sterile surgical convenience kits used in cesarean section and obstetric procedures worldwide due to equipment calibration issues that may compromise sterilization assurance.

    Product
    Medline Convenience Kits: 1) C-SECTION PACK, Model Number: CDS820080N; 2) C-SECTION CDS, Model Number: CDS983523G; 3) C-SECTION, Model Number: CDSCCR611O; 4) C-SECTION, Model Number: CDSCCR611P; 5) LUD C-SECTION-LF, Model Number: DYNJ0101616I; 6) C-SECTION TRAY, Model
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2089-2026·2026-05-13

    Medline Convenience Kits recalled due to sterilization calibration issue

    Medline is recalling two models of Convenience Kits because calibration issues with sterilization and packaging equipment may have compromised the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) ANCILLARY PACK-LF, Model Number:DYNJ0185290G; 2) OPEN HEART ANESTHESIA ICC-A, Model Number:DYNJ905567A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2026·2026-05-13

    Medline Triple Lumen Insertion Kits Recalled for Sterilization Calibration

    Medline Industries is recalling Triple Lumen Insertion Kits (Model DYNDM1031A) due to calibration issues with sterilization equipment that may have compromised the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0718-2026·2026-05-13

    Loard's Blueberry Cheesecake Ice Cream Recalled for Undeclared Milk and Dyes

    Loard's Blueberry Cheesecake Ice Cream (32 oz) is recalled due to undeclared milk, Red #40, and Blue #1. The product may pose a risk to consumers with milk allergies or sensitivities to food dyes.

    Product
    Loard's Blueberry Cheesecake Ice Cream - 32 oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0731-2026·2026-05-13

    Loard's Coffee Ice Cream Recalled for Undeclared Milk Allergen

    Silver Moon LP is recalling Loard's Coffee Ice Cream (32 oz) due to undeclared milk. Consumers with milk allergies face potential health risks.

    Product
    Loard's Coffee Ice Cream - 32 oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0752-2026·2026-05-13

    Loard's Strawberry Ice Cream recalled for undeclared milk and Red #40

    Silver Moon LP is recalling Loard's Strawberry Ice Cream (32 oz and 56 oz) distributed in Northern California due to undeclared milk and Red #40. The product poses a risk to consumers with milk allergies.

    Product
    Loard's Strawberry Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0694-2026·2026-05-13

    Woodstock Organic Shelled Edamame Recalled for Metal Contamination

    Green Organic Vegetables is recalling Woodstock Organic Shelled Edamame nationwide due to metal contamination affecting 7,160 cases in 10 oz. and 48 oz. packages. Consumers should not consume the product and should return or discard it.

    Product
    Woodstock Organic Shelled Edamame 10 oz. and 48 oz.
    Category
    Food
    Distribution
    Distributed nationwide