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.

Filters

Agency

Category

Minimum severity

Clear filters

6301–6325 of 7452

  • CriticalFDA (Devices)·Z-1756-2013·2013-07-31

    LeMaitre Recalls Albo Graft Vascular Implants Due to Surface Leaking

    LeMaitre Vascular is recalling 7 units of Albo Graft Knitted with Collagen, Bifurcate 16x08 due to blood blushing or leaking from the graft surface after implantation.

    Product
    Albo Graft Knitted with Collagen, Bifurcate 16x08 Catalog Number: AMC1608 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1791-2013·2013-07-31

    GE Healthcare Recalls Discovery NM 630 Nuclear Imaging Systems

    GE Healthcare is recalling 108 Discovery NM 630 nuclear imaging systems worldwide due to a failure mode that can cause serious injury or death.

    Product
    Discovery NM 630, dual detector free-geometry integrated nuclear imaging system. Product Usage: The GE Discovery NM 630 system is a medical tool intended for use by appropriately trained healthcare professionals to aid in detecting, localizing, diagnosing of diseases and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1761-2013·2013-07-31

    LeMaitre Vascular Recalls AlboGraft Vascular Grafts Due to Surface Leaking

    LeMaitre Vascular is recalling 3 units of AlboGraft Knitted with Collagen vascular grafts because they may leak blood from the surface after implantation.

    Product
    AlboGraft Knitted with Collagen, Straight 40x08 Catalog Number: AMC4008 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1789-2013·2013-07-31

    GE Healthcare Recalls Elscint APEX Helix Gamma Cameras Due to Patient Death

    GE Healthcare is recalling 50 Elscint APEX Helix gamma cameras worldwide after a patient died from injuries sustained during a scan at a US VA Medical Center.

    Product
    Elscint APEX Helix, dual-head, multi-purpose, Slip-Ring, digital gamma camera Product Usage: The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1742-2013·2013-07-31

    Bergin Fruit and Nut Pistachios Recalled Due to Salmonella Risk

    Bergin Fruit and Nut Co is recalling pistachio products because Salmonella was found in the environment at the supplier, ARO Pistachio Inc.

    Product
    603684 PISTACHIOS S/I/S 12/10 OZ GOLD BAG, UPC 2052603684 600913 PISTACHIOS S/I/S 12/12 OZ BAGLINE, UPC 2052600913 600913.11 PISTACHIOS S/I/S 12/12 OZ BAGLINE AMAZON, UPC 2052600913 600913.07 PISTACHIOS S/I/S 12/12 OZ BAGLINE DISPLAY BOX, UPC 2052600913 600923.05…
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Devices)·Z-1770-2013·2013-07-31

    LeMaitre Recalls AlboGraft Vascular Grafts Due to Surface Bleeding

    LeMaitre Vascular is recalling 3 units of AlboGraft Woven with Collagen, Straight 30x26 (Lot 56890A) because blood blushing or leaking was observed from the graft surface after implantation.

    Product
    AlboGraft Woven with Collagen, Straight 30x26 Catalog Number: ATC3026 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1790-2013·2013-07-31

    GE Healthcare Recalls Nuclear Medicine Imaging Systems Due to Patient Death

    GE Healthcare is recalling 13 Brivo NM615 nuclear medicine imaging systems worldwide after a patient died from injuries sustained during a scan on a related system.

    Product
    Brivo NM615, is an all-purpose, single detector integrated nuclear imaging system. Product Usage: The Brivo NM 615 is an emission computed tomography system intended to detect the location and distribution of gamma ray photon emitting radionuclides in the body and to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1788-2013·2013-07-31

    GE Healthcare Recalls Nuclear Medicine Imaging Systems Due to Patient Death

    GE Healthcare is recalling Varicam/VG and VG Hawkeye devices after a patient died from injuries sustained during a scan at a US VA Medical Center.

    Product
    GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of scanning modes supported by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1744-2013·2013-07-31

    High Quality Organics Recalls Dried Oregano Due to Salmonella Risk

    High Quality Organics is recalling dried oregano sold in 25 lb boxes because a customer's test found Salmonella in the product.

    Product
    Dried Oregano, cut and sifted; Organic; Product of Turkey, sold in 25 lb boxes High Quality Organics, Reno, NV
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1740-2013·2013-07-31

    Bergin Fruit and Nut Pistachio Recall Due to Salmonella Risk

    Bergin Fruit and Nut is recalling raw pistachio products because Salmonella was found in the environment at the supplier, ARO Pistachio Inc.

    Product
    600943 PISTACHIOS KERNELS RAW 8/11 OZ SQ TUB, UPC 2052600943 601902 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG, UPC 2052601902 601902.09 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG BYERLYS, UPC 2052601902 600899 PISTACHIOS KERNELS RAW 30#, IUPAC 600901 PISTACHIOS…
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·F-1711-2013·2013-07-24

    Fresh Unlimited Broccoli Salad Kit Recalled for Listeria Contamination

    Fresh Unlimited Inc is recalling Broccoli Salad Kit No Dressing because a supplier ingredient was linked to a Listeria monocytogenes recall.

    Product
    Broccoli Salad Kit No Dressing, packaged in plastic bags inside paper cartons, 4 bags per case.
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Devices)·Z-1691-2013·2013-07-24

    Codman MedStream Infusion Pump Recalled for Miscalibrated Fill Level Sensor

    Codman & Shurtleff is recalling MedStream Programmable Infusion Pumps because a miscalibrated fill level sensor may affect dosing levels.

    Product
    MedStream Programmable Infusion Pump , Implantable for the intrathecal delivery of Baclofen or Morphine Product Code: 91-4201US (40ml pump) 91-4201 (40ml pump) Intended for the intrathecal delivery of Baclofen or Morphine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1712-2013·2013-07-24

    Fresh Unlimited Broccoli Salad Kit Recalled for Listeria Contamination

    Fresh Unlimited Inc is recalling Broccoli Salad Kit No Dressing, No Bacon because a supplier's sunflower raisin mix was contaminated with Listeria monocytogenes.

    Product
    Broccoli Salad Kit No Dressing, No Bacon; packaged in plastic bags inside paper cartons, 4 bags per case.
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1723-2013·2013-07-24

    MR Cuts Recalls Mango Chunks Due to Salmonella Contamination Risk

    MR Cuts, L.p. is recalling Item # 2999 Mango Chunks because the product has the potential to be contaminated with salmonella.

    Product
    Item # 2999 Mango Chunks 2/5 LB, Ingredients: Mango Packed By: Riley's Dallas, Texas 75226 Product of Mexico
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1714-2013·2013-07-24

    Fresh Unlimited Recalls Sweet & Sassy Apple Salad Due to Listeria

    Fresh Unlimited Inc is recalling Sweet & Sassy Apple Salad because a supplier ingredient was linked to a Listeria monocytogenes contamination.

    Product
    Sweet & Sassy Apple Salad; packaged in plastic bags inside paper cartons, 5 bags per case.
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Devices)·Z-1690-2013·2013-07-24

    Codman MedStream Infusion Pump Recalled for Miscalibrated Fill Level Sensor

    Codman & Shurtleff is recalling MedStream Programmable Infusion Pumps because a miscalibrated fill level sensor may affect dosing levels.

    Product
    MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:91-4200 (20ml pump) US 91-4200. Intended for the intrathecal delivery of Baclofen or Morphine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1720-2013·2013-07-24

    Windy Acres Recalls Sunflower Kernel and Raisin Mix for Listeria Risk

    Windy Acres Candy & Nut is recalling a raw sunflower kernel and dark raisin mix because the supplier reported potential Listeria monocytogenes contamination.

    Product
    RAW SUNFLOWER KERNEL, DARK RAISIN 50/50 MIX 24/l0 oz packaged in clear plastic wrap.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1713-2013·2013-07-24

    Fresh Unlimited Broccoli Salad Kit Recalled for Listeria Contamination

    Fresh Unlimited Inc is recalling Broccoli Salad Kits because a supplier's sunflower raisin mix packets were contaminated with Listeria monocytogenes.

    Product
    Broccoli Salad Kit with Dressing; packaged in plastic bags inside paper cartons, 5 bags per case.
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1682-2013·2013-07-17

    Lipari Foods Recalls Shelled Pistachios Due to Listeria Contamination

    Lipari Foods, Inc. is recalling 144 cases of shelled pistachios due to potential contamination with Listeria monocytogenes. The product was distributed across nine states.

    Product
    Item Number: 201612 Item Description: BAGS SM PISTACHIO SHELLED R/S Case Pack: 12 Package Size: 0.75 OZ Fully Preprinted New Style Pic-A-Nut Bag UPC Number: 070207020217
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1667-2013·2013-07-17

    Lipari Foods Recalls Pecan Pieces Due to Listeria Contamination

    Lipari Foods is recalling 4-ounce bags of Pecan Pieces due to potential Listeria monocytogenes contamination. The product was distributed across nine states.

    Product
    Item Number: 193044 Item Description: BAGS LG PECAN PIECES Case Pack: 12 Package Size: 4 OZ Fully Preprinted Old Style Pic-A-Nut Bag UPC Number: 070207016227
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1700-2013·2013-07-17

    Lipari Foods Recalls Raw Almonds for Listeria Contamination

    Lipari Foods is recalling 15 oz tubs of raw almonds contaminated with Listeria monocytogenes. The product was distributed across nine states.

    Product
    Item Number: 374103 Item Description: TUB LG ALMOND WHOLE RAW Case Pack: 12 Package Size: 15 OZ 2-Piece Clear Plastic Tub (No Label on Top, Nutritional Label on Bottom) UPC Number: 094776081820
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1614-2013·2013-07-17

    Del Monte Recalls Fresh-Cut Mangoes Due to Salmonella Risk

    Del Monte is voluntarily recalling 1,600 bowls of fresh-cut mangoes due to a potential risk of Salmonella contamination from a specific Mexican supplier.

    Product
    Seasonal Blend: Del Monte brand, 32 oz., UPC 7-17524-77604-4; 7 Eleven brand, 6 oz., UPC 7-17524-77647-1; 16 oz., UPC 7-17524-77647-1; Wal-Mart, 10 oz., UPC 7-17524-77815-4; 16 oz., UPC 7-17524-77603-7; 32 oz., UPC 7-17524-77604-4
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1693-2013·2013-07-17

    Lipari Foods Recalls Banana Chips Due to Listeria Contamination

    Lipari Foods is recalling 10-ounce bags of banana chips due to potential Listeria monocytogenes contamination. The product was distributed across nine states.

    Product
    Item Number: 365163 Item Description: BAGS BANANA CHIPS PP Case Pack: 12 Package Size: 10 OZ Clear Plastic Bag (Black Label on Front, Nutritional Label on Back) UPC Number: 094776110186
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1694-2013·2013-07-17

    Lipari Foods Recalls Cherry Berry Delight Mix Due to Listeria Risk

    Lipari Foods is recalling 63 cases of Cherry Berry Delight mix due to potential Listeria monocytogenes contamination. The product was distributed across nine states.

    Product
    Item Number: 365172 Item Description: BAGS MIX CHERRY BERRY DELIGHT PP Case Pack: 12 Package Size: 9.5 OZ Clear Plastic Bag (Black Label on Front, Nutritional Label on Back) UPC Number: 094776110209
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1603-2013·2013-07-17

    Finger Lakes Farmstead Cheese Recalled for Listeria monocytogenes Contamination

    Finger Lakes Farmstead Cheese Company is recalling Schuyler Gouda cheese due to Listeria monocytogenes contamination. The product was distributed to one firm in New York State.

    Product
    Finger Lakes FARMSTEAD CHEESE Mecklenburg, NY Schuyler County, SCHUYLER Gouda aged at least 60 days, Net Wt. 8 lbs wheels. FINGER LAKES FARMSTEAD CHEESE CO. 5491 BERGEN ROAD TRUMANBURG, NY 14886. Ingredients: raw milk, rennet, calcium chloride, culures, salt
    Category
    Food
    Distribution
    1 state