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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33526–33550 of 39756

  • SevereNHTSA·13V589000·2013-11-22

    Maserati Recalls 2014 Quattroporte GTS for Wiring Fire Risk

    Maserati is recalling 2014 Quattroporte GTS vehicles due to a wiring defect that could cause a fire or vehicle stall.

    Product
    MASERATI — MASERATI QUATTROPORTE GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·14028·2013-11-21

    Angelcare Baby Monitors Recalled for Infant Strangulation Hazard

    Angelcare is recalling about 600,000 baby monitors in the U.S. and 182,173 in Canada due to a strangulation risk from the sensor pad cord. Two infant deaths have been reported.

    Product
    Angelcare Movement and Sound Baby Monitors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1732-2013·2013-11-20

    Priester's Pecans Roasted Nuts Recalled for Salmonella Risk

    Priester Pecan Company is recalling Fancy Roasted Nuts because pistachios supplied by ARO may be contaminated with Salmonella.

    Product
    PRIESTER'S PECANS brand FANCY ROASTED NUTS, Stock No. 7, Net Wt 12 oz (454g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1731-2013·2013-11-20

    Priester's Pecans Nutty Favorites Recalled for Salmonella Risk

    Priester Pecan Company is recalling Nutty Favorites Assortments because supplied pistachios may be contaminated with Salmonella.

    Product
    PRIESTER'S PECANS brand NUTTY FAVORITES ASST, Stock No. 79, Net Wt 1 lb 10 oz (737g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0149-2014·2013-11-20

    Empirical Labs SuperFuel Tropical Dietary Supplement Recalled for Chloramphenicol

    Empirical Labs is recalling SuperFuel Tropical dietary supplements due to potential adulteration with chloramphenicol. The product was distributed to Idaho, Minnesota, South Carolina, and Sweden.

    Product
    Empirical Labs Building Health SuperFuel Tropical Dietary Supplement
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0202-2014·2013-11-20

    Synthes 8.5 MM Medullary Reamer Recalled Due to Intraoperative Breakage

    Synthes USA HQ, Inc. is recalling 2,979 units of the 8.5 MM Medullary Reamer because the reamer head can break during surgery, leaving unretrieved fragments of non-implant grade material.

    Product
    Synthes 8.5 MM Medullary Reamer Product Usage: An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0280-2014·2013-11-20

    Stryker Recalls Acetabular Pressurizers Due to Cracked Assemblies

    Stryker is recalling 87 boxes of Acetabular Pressurizers because cracked assemblies may release during cement application.

    Product
    Acetabular Pressurizer; single use and six units per box. The Acetabular Pressurizer 0206-522-000 is an accessory to the Advanced Cement Mixer (ACM). The Acetabular Pressurizer Tiplet P/N 0206-522-012 is sealed in a two pouches, sterilized, and labeled as part number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0163-2014·2013-11-20

    Bairn Biologics Candisol Recalled Due to Chloramphenicol Contamination

    Bairn Biologics is recalling Candisol dietary supplements because the xylanase enzyme ingredient was found to be contaminated with Chloramphenicol.

    Product
    Bairn Biologics Candisol; Natural Enzymes to Support a Health Gastrointestinal Tract. Dietary Supplement; Ingredients: Vegetarian Cellulase, Vegetarian Hemicellulase, Vegetarian Xylanase, Vegetarian Beta-glucanase, microcrystalline Cellulose, L-Leucine, Vegetable Capsule.…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0175-2014·2013-11-20

    GoPicnic Hummus and Crackers Meal Kits Recalled for Undeclared Milk

    GoPicnic is recalling Hummus & Crackers meal kits because the included chocolates may contain undeclared milk allergens.

    Product
    Gopicnic; Hummus & crackers; GoPicnic meal kit packaged in paperboard container. ready-to-eat meal; with professor zim zam's extraordinary sweets dark chocolate with sea salt. NET WT 4.1 OZ (116g); distributed by gopicnic brands, inc.; chicago, il 60613; www.gopicnic.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V588000·2013-11-20

    Nissan Recalls 2014 Infiniti Q50 for Steering Software Defect

    Nissan is recalling 2014 Infiniti Q50 vehicles because freezing temperatures may disable electric steering and delay the mechanical backup, increasing crash risk.

    Product
    INFINITI — INFINITI Q50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0157-2014·2013-11-20

    Empirical Labs Recalls Greens Supplements for Chloramphenicol Contamination

    Empirical Labs is recalling specific lots of Go Green Fuel for the Entire Body dietary supplements due to potential adulteration with chloramphenicol.

    Product
    Non-GMO Ingredients Go Green Fuel for the Entire Body Dietary Supplement. All-Natural Greens Dietary Supplement. Manufactured Exclusiveley for: Hsin Ten Enterprise USA, Inc. Industry, CA 91748.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0174-2014·2013-11-20

    GoPicnic Meal Kits Recalled for Undeclared Milk Allergen

    GoPicnic is recalling Black Bean Dip & Plantain Chips meal kits because the included chocolates may contain undeclared milk allergens.

    Product
    GoPicnic Black Bean Dip & Plantain Chips; ready-to-eat meal kit with professor zim zam's extraordinary sweets dark chocolate with orange packaged in paperboard container; NET WT 4.2 OZ (116.2g); distributed by gopicnic brands, inc.; chicago, il 60613; www.gopicnic.com;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0205-2014·2013-11-20

    Hospira Recalls Plum A+ Infusion Pumps Due to Pressure Sensor Drift

    Hospira is recalling 71 Plum A+ Infusion Pumps because pressure sensor calibration drift can cause false alarms or missed occlusions.

    Product
    Plum A+ Infusion Pump; List Number: 11973; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0186-2014·2013-11-20

    Fresenius Medical Care Recalls Combiset Blood Lines for Hemodialysis

    Fresenius Medical Care is recalling 508,029 cases of Combiset Blood Lines for hemodialysis because connections may disconnect if not tightened correctly, leading to blood loss.

    Product
    Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0144-2014·2013-11-20

    Apex Energetics Recalls Four Enzyme Supplements Due to Chloramphenicol Contamination

    Apex Energetics is recalling four enzyme-based dietary supplements because they may contain trace amounts of the antibiotic chloramphenicol.

    Product
    RepairVite (K63), Enzyme-Based Herbal & Amino Acid Dietary Supplement Powder, Caramel Flavor, Net Wt. 0.34 lb (155g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0158-2014·2013-11-20

    ProThera Recalls Serralase Enzyme Supplements Due to Chloramphenicol Contamination

    ProThera, Inc. is recalling Serralase Enzyme Supplements because the enzymes used may be contaminated with chloramphenicol.

    Product
    Serralase Enzyme Supplements; Packaged in 90 and 180 tablet bottled UPC - 90 count: 8 28054 00542 6 UPC- 180 count 8 28054 00149 7; Manufactured by: ProThera, Inc., Reno, NV 89521
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·13V582000·2013-11-20

    Jet Co Aluminum Grain Trailers Recalled for Weak Top Rail

    Jet Co is recalling 2011-2012 aluminum grain trailers because a weak top rail may buckle, increasing crash risk.

    Product
    JET CO — JET CO ALUMINUM GRAIN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide