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.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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36201–36225 of 39777

  • SevereFDA (Food)·F-0035-2013·2012-10-17

    Cut Fruit Express Recalls Cantaloupe, Pineapple, and Watermelon Mix

    Cut Fruit Express, Inc. is recalling 15-ounce fruit mix containers due to a positive Salmonella sample found in processed cantaloupe.

    Product
    CANTALOUPE, PINEAPPLE AND WATERMELON: H.Brooks & Company 33531 FRUIT MIX CPW SPEARS 15oz (425g) 4 per case UPC# 0 3823233531 7. Distributed by H. Brooks & Co Mpls. MN55112.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0051-2013·2012-10-17

    Terumo Sarns Centrifugal System Control Module Recalled for Power Loss

    Terumo CVS is recalling Sarns Centrifugal System Control modules due to a report of power loss during cardiopulmonary bypass.

    Product
    Sarns Centrifugal System Control module, 100/115V The Sarns Centrifugal System is indicated for use in cardiopulmonary bypass procedures only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0083-2013·2012-10-17

    United Salad Company Recalls Mango Salsa Due to Salmonella Risk

    United Salad Company is recalling specific mango salsa products because the mangos used may be contaminated with Salmonella. The products were distributed to wholesale and retail customers in five western states.

    Product
    Mango Salsa 1) Garden Highway Plant Code: P-002 brand Mango Salsa 9 oz UPC 826766-422005 2) Mary's Select brand Tropical Salsa 16 oz UPC 9250474578 3) Mary's Select brand Tropical Salsa 16 oz UPC 9250474569 4) Garden Highway Plant Code: P-002 brand Salsa Tropical Fresh…
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0036-2013·2012-10-17

    Cut Fruit Express Recalls Cantaloupe and Honeydew Due to Salmonella

    Cut Fruit Express, Inc. is recalling processed cantaloupe and honeydew products due to a positive Salmonella sample found by the supplier.

    Product
    CANTALOUPE, HONEYDEW: Festival Foods-Best Of The Season 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. H.Brooks 46981 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. Distributed by H.…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0097-2013·2012-10-17

    Manna Organics Recalls Soybean Sprouts Due to Listeria Risk

    Manna Organics Inc. is recalling SooNyeoWon Soybean Sprouts in 5 lb, 10 lb, and 16 oz packages due to potential Listeria monocytogenes contamination.

    Product
    SooNyeoWon Soybean Sprouts (5 lbs., 10 lbs., and 16-ounce packages - all packaged in plastic bags). 16-oz bag UPC 0 28346 07121 8; Manna Organics Inc. 170 Avenue 'L', Newark, NJ 07105; MSB West, LLC 622 South Anderson Street, Los Angeles, CA 90023
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0013-2013·2012-10-17

    Baxter Buretrol Solution Set Recalled Due to Ball-Valve Malfunction

    Baxter Healthcare is recalling Buretrol Solution Sets because the ball-valve feature may allow air to flow into the tubing.

    Product
    Baxter Interlink System Buretrol Solution Set, 117" (3.0 m), with 150 mL Burette (Ball-Valve Drip Chamber) (Non-DEHP); a sterile Rx IV fluid pathway device; Product Usage: The device is used for the administration of fluids from a container into the patient's vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0027-2013·2012-10-17

    OrthoHelix 3.8mm Cannulated Hex Drivers Recalled for Tip Breakage

    Orthohelix Surgical Designs Inc is recalling 120 non-sterile 3.8mm cannulated hex drivers because the tips break while driving screws into patients.

    Product
    OrthoHelix Part #HCS-056-32 3.8MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in the Mini MaxTorque Screw System, which is intended to be used to stabilize and aid in the fusion of fractures and osteotomies involving small bones of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0015-2013·2012-10-17

    Baxter Recalls Clearlink System Buretrol Solution Sets Due to Valve Malfunction

    Baxter Healthcare is recalling 488,504 units of Clearlink System Buretrol Solution Sets because the ball-valve feature may allow air to enter the tubing.

    Product
    Baxter Clearlink System Buretrol Solution Set, 115" (2.9 m) with 150 mL Clearlink Burette (Ball-Valve Drip Chamber) (Non-DEHP); a sterile Rx IV fluid pathway device Product Usage: The device is used for the administration of fluids from a container into the patient's…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0053-2013·2012-10-17

    Terumo Sarns Centrifugal System Control Module Recalled for Power Loss

    Terumo CVS is recalling Sarns Centrifugal System Control modules due to a report of power loss during cardiopulmonary bypass.

    Product
    Sarns Centrifugal System Control module System 9000 The Sarns Centrifugal System is indicated for use in cardiopulmonary bypass procedures only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0017-2013·2012-10-17

    Accutron Recalls Flowmeter Assemblies for Incorrect Nitrous Gas Function

    Accutron is recalling specific Flowmeter assemblies used in analgesia gas machines because they function incorrectly when nitrous gas flows without oxygen.

    Product
    Flow Meter, CM Assembly, Model #27025, Serial # 13686, 13690, 13712, 13793. Flowmeter, CM Assembly, Model#31970, Serial#13692. Product Usage: Conscious Sedation Unit Analgesia Gas Machine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0049-2013·2012-10-17

    Terumo Sarns Centrifugal System Battery Backup Recall for Malfunctions

    Terumo CVS is recalling Sarns Centrifugal System batteries due to reports of charging and operational failures that could cause loss of arterial flow.

    Product
    Battery, 100/115V (Includes charger and connecting cable) The Sarns" Centrifugal System is indicated for use in cardiopulmonary bypass procedures only.
    Category
    Medical Device
    Distribution
    43 states
  • SevereFDA (Food)·F-0046-2013·2012-10-17

    3fish Inc. Recalls Stuffed Tilapia Due to Listeria Contamination

    3fish Inc. is recalling Harris Teeter Stuffed Tilapia 8ct (Fresh) because it was manufactured with diced onions contaminated with Listeria monocytogenes.

    Product
    Harris Teeter, Stuffed Tilapia 8ct (Fresh)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0012-2013·2012-10-17

    Baxter Buretrol Solution Set Recalled for Potential Air Inflow

    Baxter is recalling Buretrol Solution Sets because the ball-valve feature may allow air to flow into the tubing at the completion of a dose.

    Product
    Baxter Interlink System Buretrol Solution Set with 150 mL Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0091-2013·2012-10-17

    G.O. Fresh Recalls Cantaloupe Fruit Mix Chunks Due to Salmonella Risk

    G.O. Fresh is voluntarily recalling specific cut fruit mix chunks containing cantaloupe due to potential Salmonella contamination linked to a DFI Marketing recall.

    Product
    SYSCO Imperial 6520795 1/5# FRUIT MIX CHUNKS 3/4" 130249 & 130250 BEST BY 9/15/12 & 9/16/12, UPC# 1007 4865393314.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0032-2013·2012-10-17

    Cut Fruit Express Recalls Melon Mix Slices Due to Salmonella Risk

    Cut Fruit Express is recalling melon mix slices because the supplier recalled processed cantaloupe after a positive Salmonella sample.

    Product
    CANTALOUPE, WATERMELON, HONEY DEW, RED GRAPES: Festival Foods-Best Of The Season 30787 H.Brooks Melon Mix Slices Net Wt. 12 oz. (340g) 3 units per case 331 UPC# 0 3823230787 1.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0104-2013·2012-10-17

    Manna Organics Soon Tofu Recalled for Potential Listeria Contamination

    Manna Organics Inc. is recalling Soon Tofu due to potential contamination with Listeria monocytogenes. The product was distributed in ten states.

    Product
    Soon Tofu, 30-pieces packaged in large, white, plastic bucket. Manna Organics Inc. Newark, NJ
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0085-2013·2012-10-17

    Kroger Fresh Selections Tender Spinach Recalled for Listeria

    Kroger is recalling Fresh Selections Tender Spinach after the Ohio Department of Agriculture detected Listeria monocytogenes in the product.

    Product
    FRESH SELECTIONS by Kroger" Tender Spinach NET WT 10 OZ (283g) BEST IF USED BY 09/16/12 Product of USA 10:09 HarvestMark.com, 1104 A244 0105 KN01 INGREDIENTS: SPINACH DISTRIBUTED BY THE KROGER COM. CINCINNATI OHIO 45202
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-0090-2013·2012-10-17

    G.O. Fresh Recalls Cut Fruit Mix Due to Salmonella Risk

    G.O. Fresh is voluntarily recalling specific cut fruit mix items containing cantaloupe due to potential Salmonella contamination.

    Product
    SYSCO Imperial 4835718 30/4.5 OZ FRUIT MIX CANT/PINE/REDGRAPES 130249 & 130250 BEST BY 9/15/12 & 9/16/12. SYSCO Imperial 7068657 4/5# FRUIT MIX CANT/PINE/RED GRAPE 130250 BEST BY 9/16/12.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0098-2013·2012-10-17

    Manna Organics Firm Tofu Recalled for Listeria Contamination Risk

    Manna Organics is recalling SooNyeoWon and Jinga brand Firm Tofu due to potential Listeria monocytogenes contamination. The product was distributed in ten states.

    Product
    SooNyeoWon and Jinga brand Firm Tofu; Net Wt. 16 oz., in square white plastic container, UPC 0 28346 07812 5 and 0 28346 09112 4, respectively. Manna Organics Inc. 170 Avenue 'L', Newark, NJ 07105; MSB West, LLC 622 South Anderson Street, Los Angeles, CA 90023
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0028-2013·2012-10-17

    Remington Medical Recalls Sterile Prostate Biopsy Needles Due to Sterility Concerns

    Remington Medical Inc. is recalling 800 sterile automatic cutting needles for prostate biopsies because the product's sterility may be compromised.

    Product
    Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0026-2013·2012-10-17

    OrthoHelix 3.2mm Cannulated Hex Driver Recall Due to Tip Breakage

    Orthohelix Surgical Designs Inc is recalling 47 non-sterile 3.2mm cannulated hex drivers because their tips are breaking while driving screws into patients.

    Product
    OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in the Mini MaxTorque Screw System, which is intended to be used to stabilize and aid in the fusion of fractures and osteotomies involving small bones of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0040-2013·2012-10-17

    3fish Inc. Recalls Crab Stuffing Bucket Due to Listeria Contamination

    3fish Inc. is recalling 5 lb tubs of Crab Stuffing Bucket because they were manufactured with diced onions contaminated with Listeria monocytogenes.

    Product
    Crab Stuffing  Bucket (fresh and frozen), #84480, 5 lb Tub, Net St: 5 lbs, Packed by 3fish, Inc.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0103-2013·2012-10-17

    Manna Organics Healthy Tofu Recalled for Listeria Contamination Risk

    Manna Organics Inc. is recalling Healthy Tofu products due to potential Listeria monocytogenes contamination. The recall affects units distributed across ten states.

    Product
    Labeled in Korean as Healthy Tofu, 5-pieces and 10 pieces, UPC 028346091292. Manna Organics Inc. Newark, NJ.
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0102-2013·2012-10-17

    Manna Organics Recalls Silken Tofu Due to Listeria Risk

    Manna Organics Inc. is recalling 14 oz. containers of SooNyeoWon Silken Tofu because the product has the potential to be contaminated with Listeria monocytogenes.

    Product
    SooNyeoWon Silken Tofu; 14 oz. plastic container, UPC 0 28346 09113 1. Manna Organics Inc. 170 Avenue 'L', Newark, NJ 07105; MSB West, LLC 622 South Anderson Street, Los Angeles, CA 90023
    Category
    Food
    Distribution
    10 states
  • SevereNHTSA·12V507000·2012-10-17

    Navistar Recalls 2013 International Trucks Due to Steering Wheel Weld Defect

    Navistar is recalling 2013 International LoneStar, ProStar, and WorkStar trucks because the steering wheel may not be fully welded to its hub, risking loss of vehicle control.

    Product
    INTERNATIONAL — INTERNATIONAL WORKSTAR, LONESTAR, PROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide