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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35826–35850 of 39777

  • SevereFDA (Devices)·Z-0177-2013·2012-11-07

    Ventlab Premium Small Child Resuscitator Recalled for Valve Leakage

    Ventlab Corporation is recalling 14,602 Premium Small Child Resuscitators due to possible volume leakage through the inlet valve during compressions.

    Product
    Ventlab Premium Small Child Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0169-2013·2012-11-07

    Elekta MOSAIQ Medical Record System Recalled for Treatment Data Error

    Elekta, Inc. is recalling MOSAIQ electronic medical record systems because a user error led to a patient being seriously mistreated.

    Product
    MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR) used for oncology workflow management. It lets users supply electronic patient charts and assemble care plans, order diagnostic tests, and prescribe medications. It also lets users import, view…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0180-2013·2012-11-07

    Ventlab AirFlow Infant Resuscitator Recalled for Inlet Valve Leakage

    Ventlab is recalling 14,602 AirFlow Infant Resuscitators because the inlet valve may leak air during compressions, potentially compromising respiratory support.

    Product
    AirFlow, Infant Resuscitator, AF3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0178-2013·2012-11-07

    Ventlab Premium Small Adult Resuscitator Recalled for Valve Leakage

    Ventlab Corporation is recalling 14,602 Premium Small Adult Resuscitators due to a defect that may cause volume leakage through the inlet valve during use.

    Product
    Ventlab Premium Small Adult Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0175-2013·2012-11-07

    Ventlab AirFlow Resuscitator Recalled for Inlet Valve Leakage

    Ventlab Corporation is recalling 14,602 AirFlow Resuscitators due to possible volume leakage through the inlet valve during bag compressions.

    Product
    AirFlow Resuscitator, Adult Resuscitator, AF1000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0124-2013·2012-11-07

    HeartSine Samaritan 300/300P PAD Devices Recalled for Malfunction

    Heartsine is recalling 81,982 Samaritan 300/300P PAD devices because they may turn on or off unexpectedly, potentially preventing therapy delivery during cardiac arrest.

    Product
    HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753; 10C00200000 to 10C00210106 Product Usage: Samaritan 300/300P PAD is indicated for use on victims of sudden cardiac arrest who are exhibiting the following…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0577-2013·2012-11-07

    Xan Confections Recalls Dark Peanut Butter Cups Due to Salmonella Risk

    Xan Confections is voluntarily recalling 13 gourmet peanut butter chocolate products, including Dark Peanut Butter Cups, due to potential Salmonella contamination from a supplier.

    Product
    Chocolate, confections. Bulk Dark Peanut Butter Cup, item number 273. 24 pieces per case.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0176-2013·2012-11-07

    Ventlab Safe Spot Infant Resuscitator Recalled for Valve Leakage

    Ventlab is recalling Safe Spot Infant Resuscitators due to possible volume leakage through the inlet valve during use.

    Product
    Safe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0558-2013·2012-11-07

    Ma Baensch Marinated Herring Recalled for Undeclared Milk Allergen

    Wild Foods, Inc. is recalling 144 jars of Ma Baensch Marinated Herring in Wine Sauce due to a labeling error involving an undeclared milk allergen.

    Product
    Ma Baensch Marinated Herring in Wine Sauce, Net Wt. 24 oz.. (680g), UPC 714449-10220 in glass jars with gold metal lids.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0181-2013·2012-11-07

    Ventlab AirFlow Resuscitator Recalled for Possible Volume Leakage

    Ventlab Corporation is recalling specific lots of AirFlow Small Adult Resuscitators due to possible volume leakage through the inlet valve during compressions.

    Product
    AirFlow, Small Adult Resuscitator, AF5000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0179-2013·2012-11-07

    Ventlab Infant Resuscitator Recalled for Possible Volume Leakage

    Ventlab Corporation is recalling 14,602 infant resuscitators due to possible volume leakage through the inlet valve during bag compressions.

    Product
    Ventlab Rescue Med Infant Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0173-2013·2012-11-07

    Ventlab V*Care Infant Resuscitator Recalled for Potential Volume Leakage

    Ventlab Corporation is recalling V*Care Infant Resuscitators due to a possible volume leakage through the inlet valve during compressions.

    Product
    V*Care Resuscitator Infant Resuscitator, VN 3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V533000·2012-11-06

    Mercedes-Benz Recalls 2012 CLS550 Vehicles for Hood Latch Bolt Issue

    Mercedes-Benz is recalling 2012 CLS550 and CLS550 4Matic vehicles because insufficiently tightened hood latch bolts could allow the hood to open while driving, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V532000·2012-11-06

    Airstream Recalls 2006-2009 Classic RVs Due to Brake Hose Defect

    Airstream is recalling 2006-2009 Classic recreational vehicles because brake hoses may fail, reducing braking performance and increasing crash risk.

    Product
    AIRSTREAM — AIRSTREAM CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V534000·2012-11-06

    Mitsubishi Fuso Trucks Recalled for Parking Brake Cable Nut Issue

    Mitsubishi Fuso is recalling 2012-2013 trucks because the parking brake cable nut may be loose, risking vehicle rollaway.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC72, FEC52, FEC92, FGB72
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12E052000·2012-11-05

    Gates Super-Vac Hoses Recalled for Gasoline Leak Risk in Modified Vehicles

    Hydraulic Supply Co. is recalling Gates Super-Vac hoses used in vehicle modifications for disabled drivers because they are unsuitable for gasoline and may leak.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12C004000·2012-11-02

    Britax Recalls Convertible Child Seats Due to Choking Hazard

    Britax is recalling specific convertible child seats because the chest pads may be chewed into pieces, creating a choking hazard.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·13022·2012-11-01

    Bose Recalls Dual-Voltage CineMate II Speaker Systems Due to Fire Hazard

    Bose is recalling approximately 20,500 dual-voltage CineMate II home theater speaker systems because a component in the bass module can fail and ignite when used in 220-volt outlets.

    Product
    Dual-Voltage CineMate II Home Theater Speaker Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0446-2013·2012-10-31

    Sunland Recalls Organic Crunchy Peanut Butter Due to Salmonella Risk

    Sunland, Inc. is recalling Natural Value Organic Crunchy Peanut Butter because the products may be contaminated with Salmonella.

    Product
    Natural Value Organic Crunchy Peanut Butter, 5 lb UPC 909064; 15 lbs UPC 909101.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0363-2013·2012-10-31

    Sunland Recalls Peanut Butter Products Due to Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling specific peanut butter products, including Sprouts Farmers Market brand, due to potential Salmonella contamination.

    Product
    Sprouts Farmers Market Crunchy Peanut Butter, 16 oz, UPC 7487500337, Manufactured Exclusively for Sprouts Farmers Market, Phoenix, Arizona 85028.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0341-2013·2012-10-31

    Sunland Recalls Almond, Peanut, and Cashew Butter Products for Salmonella Risk

    Sunland, Inc. is voluntarily recalling almond, peanut, and cashew butter products and tahini due to potential Salmonella contamination.

    Product
    Joseph's Salt-Free No Sugar Added New Crunchy Valencia Peanut Butter, 18 oz, UPC 3307915073, labeling is green white red and yellow with red, white, black, and green print writing. Manufactured for: Joseph's Lite Cookies 9422 N. US Hwy 1, Sebastian, FL 32958 USA.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0344-2013·2012-10-31

    Sunland Recalls Peanut Butter Products Due to Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling specific peanut, almond, and cashew butter products because they may be contaminated with Salmonella.

    Product
    Natural Value Crunchy Peanut Butter/Salt, Product of the USA, Net Wt. 15 lbs, UPC 910060. Labeling is white with black print writing.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0335-2013·2012-10-31

    Sunland Recalls Peanut Butter Products Due to Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling specific peanut butter products, including Fresh and Easy brand, because they may be contaminated with Salmonella.

    Product
    Fresh and Easy Crunchy Peanut Butter, 18 oz, packed in plastic jars with a plastic screw on lid, UPC 20003371; labeling is red, yellow, and white with yellow, white, and black print writing. Produced for Fresh and Easy Neighborhood Market Inc, El Segundo, CA 90245.
    Category
    Food
    Distribution
    0 states