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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11001–11025 of 36632

  • SevereFDA (Food)·F-1120-2020·2020-07-22

    Fresh Express Marketside Chopped Salad Kit Recalled for Cyclospora Risk

    Fresh Express is recalling Marketside Chopped Salad Kits due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.

    Product
    Marketside Chopped Salad Kit Cherry Almond Gorgonzola 13.8 oz., UPC 681131148375, Green & red cabbage, kale, romaine lettuce, green onions & carrots
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2601-2020·2020-07-22

    Skeletal Kinetics Recalls Craniosculpt Flow Bone Void Filler Kits

    Skeletal Kinetics is recalling Craniosculpt Flow bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.

    Product
    CRANIOSCULPT FLOW, 10CC. Product Number: C-FLOW10CC, UDI: 813845020368 - - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2568-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America, LLC is recalling CMExpress Microbore Sets because they may deliver fluids with significant inaccuracy, potentially causing over-infusion or under-infusion of therapy.

    Product
    CMExpress Microbore Set, REF: A120-160CRV
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1071-2020·2020-07-22

    Fresh Express Iceberg Garden Salads Recalled for Cyclospora Risk

    Fresh Express is recalling Iceberg Garden salad products due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected lots.

    Product
    Fresh Express Iceberg Garden / Lechuga Repollo 12 oz., UPC 071279103020, (Canada UPC) 0 71279 10302 0, Green and red cabbage, kale, green leaf & Carrots. Fresh Express Iceberg Garden / Lechuga Repollo 24 oz., UPC 071279104119, (Canada UPC) 0 71279 10411 9, Iceberg lettuce…
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2560-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Administration Sets

    CME America is recalling BodyGuard Microset infusion administration sets due to delivery inaccuracy that could cause over-infusion or under-infusion of therapy.

    Product
    BodyGuard Microset, REF: A100-163XSFL
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Drugs)·D-1385-2020·2020-07-22

    Lupin Recalls Metformin Hydrochloride Tablets Due to NDMA Impurity

    Lupin Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-1129-2020·2020-07-22

    Fresh Express Marketside Kale Slaw Recalled for Cyclospora Risk

    Fresh Express is recalling Marketside Kale Slaw due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.

    Product
    Marketside Kale Slaw 12 oz., UPC 681131221573, Broccoli stalks, kale, radicchio, carrots & red cabbage
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2584-2020·2020-07-22

    CME America BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets because they may deliver fluid at inaccurate rates, potentially causing over- or under-infusion of therapy.

    Product
    BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer, REF: A120-160XYBF
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1135-2020·2020-07-22

    Fresh Express Signature Farms Coleslaw Recalled for Cyclospora Risk

    Fresh Express is recalling Signature Farms Coleslaw 3 Color 14 oz. due to a possible health risk from Cyclospora.

    Product
    Signature Farms Coleslaw 3 Color 14 oz., UPC 021130111691, Green & red cabbage and carrots
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1076-2020·2020-07-22

    Fresh Express Premium Slaw Salad Kit Recalled for Cyclospora Risk

    Fresh Express is recalling Premium Slaw Salad Kit Asian Avocado products due to a possible health risk from Cyclospora.

    Product
    Fresh Express Premium Slaw Salad Kit Asian Avocado 9.7 oz., UPC 071279126043, Romaine lettuce & red cabbage
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2611-2020·2020-07-22

    Medtronic Bone Void Filler Recalled for Potential Failure to Set Properly

    Skeletal Kinetics is recalling Medtronic Bone Void Filler kits that may not maintain setting characteristics, potentially increasing surgical time or causing bone formation issues.

    Product
    MEDTRONIC BONE VOID FILLER, SMALL. Product Number: C07A, UDI: 813845020504 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2563-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Administration Sets

    CME America is recalling BodyGuard Microset infusion administration sets due to delivery inaccuracy that could cause over-infusion or under-infusion of therapy.

    Product
    BodyGuard Microset, REF: A120-161XYBS
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1065-2020·2020-07-22

    Fresh Express Farmer's Garden Salad Recalled for Cyclospora Risk

    Fresh Express is recalling Farmer's Garden salads due to a possible health risk from Cyclospora. Consumers should check their refrigerators for the affected product.

    Product
    Fresh Express Farmer's Garden 9 oz., UPC 071279281025, Butter & red leaf lettuce, grape tomatoes, carrots & radishes
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2583-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Sets Due to Delivery Inaccuracy

    CME America is recalling 6,320 BodyGuard Microset infusion sets because they may deliver fluids with significant inaccuracy, potentially causing over- or under-infusion of therapy.

    Product
    BodyGuard Microset with Filter and Manual Priming Valve, REF: A120-112XSFV
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2613-2020·2020-07-22

    Skeletal Kinetics Recalls Osteovation EX Bone Void Filler Kits

    Skeletal Kinetics is recalling Osteovation EX bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.

    Product
    OSTEOVATION EX, 5CC, IMPACT FORMULA. Product Number: 390-0205, UDI: 813845020047 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1115-2020·2020-07-22

    Fresh Express Little Salad Bar Southwest Chopped Salad Kit Recalled for Cyclospora Risk

    Fresh Express is recalling Little Salad Bar Southwest Chopped Salad Kits due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.

    Product
    Little Salad Bar Southwest Chopped Salad Kit 12 oz., UPC 4099100087024, Green and red cabbage, green leaf lettuce, carrots & green onion
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2588-2020·2020-07-22

    CME BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets because they may deliver therapy at inaccurate rates, potentially causing over- or under-infusion.

    Product
    BodyGuard Microset With Female Luer, REF: A120-160XPSN
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2589-2020·2020-07-22

    CME BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets due to potential delivery inaccuracies that could cause over- or under-infusion of therapy.

    Product
    BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer, REF: A120-160CYFRV
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2579-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America is recalling 4,234 CMExpress Microbore Sets because they may deliver fluids with significant inaccuracy, potentially causing over- or under-infusion of therapy.

    Product
    CMExpress Microbore Sets, REF: A120-160C2YRV
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Drugs)·D-1384-2020·2020-07-22

    Lupin Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity

    Lupin Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1383-2020·2020-07-22

    Lupin Recalls Metformin Hydrochloride Tablets Due to NDMA Impurity

    Lupin Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-1128-2020·2020-07-22

    Fresh Express Marketside Crisp Greens Recalled Due to Cyclospora Risk

    Fresh Express is recalling Marketside Crisp Greens 12 oz. due to a possible health risk from Cyclospora. Consumers should not consume the product.

    Product
    Marketside Crisp Greens 12 oz., UPC 681131387552, Romaine lettuce, red cabbage, iceberg lettuce & carrots
    Category
    Food
    Distribution
    32 states