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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14376–14400 of 36682

  • SevereFDA (Drugs)·D-1090-2019·2019-04-17

    FDA Recalls Compounded Penile Injection Drugs Due to Insanitary Conditions

    Professional Compounding Pharmacy is recalling compounded papaverine-phenolamine-PGE1 injections due to insanitary conditions observed during an FDA inspection.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 22-0.8 MG-8 MCG/ML* INJECTABLE, (a) 5ml (b) 10ml, (c) 6ml, penile injection, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1095-2019·2019-04-17

    FDA Recalls Compounded Papaverine-Phentolamine-PGE1 Injectable Due to Insanitary Conditions

    Professional Compounding Pharmacy is recalling specific lots of compounded Papaverine-Phentolamine-PGE1 injectable because FDA inspectors observed insanitary conditions during the compounding process.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 17.16-0.57MG-19.45MCG/ML* INJECTABLE, 5ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1083-2019·2019-04-17

    Losartan Potassium Tablets Recalled Due to Nitrosamine Impurity

    Pharma Pac is recalling Losartan Potassium 100 mg tablets because traces of a nitrosamine impurity were found in the active ingredient.

    Product
    Losartan Potassium 100 mg Tablets # 30 Losartan potassium tablets USP, 100 mg are white to off white, film coated, tear drop shaped tablets, debossed with "H" on one side and "145" on the other side.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1248-2019·2019-04-17

    Aurobindo Recalls MARBETA L KIT Vials Due to Particulate Matter

    Aurobindo Pharma USA Inc. is recalling 88,600 vials of MARBETA L KIT because one vial was found to contain a hair.

    Product
    MARBETA L KIT — MARBETA L KIT (BETAMETHASONE SODIUM PHOSPHATE, BETAMETHASONE ACETATE, LIDOCAINE HYDROCHLORIDE, BUPIVACAINE HYDROCHLORIDE, POVIDINE IODINE, ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1104-2019·2019-04-17

    FDA Recalls Compounded Injectable Drug Due to Insanitary Compounding Conditions

    Professional Compounding Pharmacy is recalling Papaverine-Phentolamine-PGE1 injectable due to insanitary conditions observed during compounding.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 17.64-0.58MG-5.88MCG/ML* INJECTABLE, 9 ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330 .
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1094-2019·2019-04-17

    Professional Compounding Pharmacy Recalls Papaverine-Phentolamine-PGE1 Injectable Due to Insanitary Conditions

    Professional Compounding Pharmacy is recalling specific lots of Papaverine-Phentolamine-PGE1 Injectable because FDA inspectors observed insanitary conditions during the compounding of sterile drugs.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 12-1MG-10MCG/ML INJECTABLE, (a) 10ml, (b) 9ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1106-2019·2019-04-17

    FDA Recalls Compounded Injectable Drug Due to Insanitary Compounding Conditions

    Professional Compounding Pharmacy is recalling a compounded injectable drug because FDA inspectors observed insanitary conditions during its compounding.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 9-1 MG-10 MCG/ML* INJECTABLE, 18 ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330 .
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·19V304000·2019-04-17

    Spartan Recalls 2019 Utilimaster Truck Bodies Due to Electrical Fire Risk

    Spartan Motors is recalling 2019 Utilimaster Truck Bodies because undersized wires may overheat, melt, and cause an unexpected engine shutdown, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V308000·2019-04-17

    Volvo Recalls 2016 XC90 Vehicles for Coolant Hose Fire Risk

    Volvo is recalling 2016 XC90 vehicles because a coolant hose may crack and leak, potentially causing a fire in the catalytic converter area.

    Product
    VOLVO — VOLVO XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1102-2019·2019-04-17

    FDA Recalls Compounded Papaverine-Phentolamine-PGE1 Injectable Due to Insanitary Conditions

    Professional Compounding Pharmacy is recalling a compounded sterile injectable drug due to insanitary conditions observed during an FDA inspection.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 15-0.5MG-10MCG/ML INJECTABLE, 9ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330 .
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·19V306000·2019-04-16

    2019 Fleetwood and Holiday Rambler Motorhomes Recalled for Exhaust Defect

    REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, ADMIRAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·19105·2019-04-12

    Fisher-Price Recalls Rock 'n Play Sleepers Due to Infant Death Reports

    Fisher-Price is recalling all Rock 'n Play Sleepers because over 30 infant fatalities have occurred. Consumers should stop using the product immediately and contact the company for a refund.

    Product
    All Models of Rock 'n Play Sleeper
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V298000·2019-04-12

    Honda and Acura Recall Vehicles Due to Timing Belt Defect

    Honda is recalling specific 2018-2019 Acura and Honda vehicles because timing belt teeth may separate, potentially causing an engine stall and increasing crash risk.

    Product
    HONDA — HONDA, ACURA PILOT, TLX, ODYSSEY, RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V299000·2019-04-12

    Honda Recalls 2018-2019 Odyssey for Transmission Control Unit Reboot Risk

    Honda is recalling 2018-2019 Odyssey vehicles because loose battery connections may cause the transmission to shift to Park, potentially damaging the parking rod and increasing crash risk.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E028000·2019-04-12

    Cush Corp Recalls Trailer Axles Due to Wheel Separation Risk

    Cush Corp is recalling specific trailer suspension systems because a locking device may not be installed properly, allowing the wheel end to separate from the axle.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·046-2019·2019-04-12

    Denver Processing Recalls Raw Pork and Beef Produced Without Inspection

    Denver Processing LLC is recalling raw pork and beef products produced without federal inspection. The products were distributed to retail locations in five states.

    Product
    JBS USA — Denver Processing LLC Recalls Raw Pork and Beef Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·19V293000·2019-04-11

    Chrysler Recalls 2013-2016 Dodge Dart Vehicles for Shifter Cable Defect

    Chrysler is recalling 2013-2016 Dodge Dart vehicles with 6-speed automatic transmissions because the shifter cable bushing may fail, allowing the cable to detach and increasing crash risk.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V296000·2019-04-11

    Karma Revero Recall: Side Air Bags May Not Deploy in Rollover

    Karma Automotive is recalling 2018 Revero vehicles because side curtain air bags may not deploy in a rollover crash due to a disabled sensor system.

    Product
    KARMA — KARMA REVERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V297000·2019-04-11

    Subaru Recalls Vehicles Due to Ignition Switch Spring Failure Risk

    Subaru is recalling specific 2005-2014 models because a broken spring in the ignition switch could cause the engine to turn off unexpectedly, increasing crash risk.

    Product
    SUBARU — SUBARU LEGACY, OUTBACK, IMPREZA, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0977-2019·2019-04-10

    O-Two Medical e600 Ventilator Recalled for Fire Risk

    O-Two Medical is recalling 119 e600 Automatic Transport Ventilators because a manufacturing defect may cause the unit to catch fire.

    Product
    e600 Automatic Transport Ventilator, Model Number 01EVE600
    Category
    Medical Device
    Distribution
    8 states