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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13401–13425 of 36664

  • CriticalFDA (Food)·F-2093-2019·2019-09-04

    FDA Recalls Fresh Basil Tested Positive for Salmonella

    Harvest Sensations, LLC is recalling fresh basil that tested positive for Salmonella. The product was imported from Mexico and distributed in New York.

    Product
    Fresh basil packaged in plastic bags, each weighing one pound. (No label)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2386-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc. is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393420, 14.5F, Straight, 42cm length, BARD, UDI: 00801741012228
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Devices)·Z-2378-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913230, 16F, Straight, 23cm length, BARD, UDI: 00801741013843
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Food)·F-2094-2019·2019-09-04

    AWERS Grained Salmon Caviar Recalled for Potential Botulism Contamination

    AWERS Inc is recalling Grained Salmon Caviar due to potential Clostridium botulinum contamination. Consumers should check their refrigerators for the specific product details.

    Product
    Grained Salmon Caviar 95g (Sockeye Salmon Caviar), refrigerated, packed in a metal tin with Cyrillic lettering. The tin is green, with red and white writing with an easy open pull lid. UPC 8 85202 00044 3. The label is read in parts: "***GRAINED SALMON CAVIAR ***INGREDIENTS…
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1845-2019·2019-09-04

    Pfizer Recalls Relpax Tablets Due to Microbial Contamination

    Pfizer is recalling specific lots of Relpax (eletriptan HBr) tablets because they may be contaminated with Burkholderia and Pseudomonas bacteria.

    Product
    RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b) 12-count (2 cards x 6 tablets) per carton, NDC 0049-2340-05, Rx only, Made in Ireland, Distributed by Pfizer Roerig, Division of Pfizer Inc., NY, NY 10017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2089-2019·2019-09-04

    Confectionery Arts International Recalls Jewel Dust Pearlescent Pigment

    Confectionery Arts International is recalling Jewel Dust pearlescent pigment because borosilicate glass material was found in an FDA sample.

    Product
    All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and sold prior to 4/25/19; 4g packed in 1/4 oz. jars and 14g packed in 1 oz. jars.
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Devices)·Z-2367-2019·2019-09-04

    Siemens Artis X-Ray Systems Recalled for Patient Table Cracks

    Siemens is recalling 17 Artis zee and Artis Q interventional X-ray systems because cracks in the patient table mainframe could cause the upper bed to detach, posing a hazard to patients and staff.

    Product
    Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material Number Artis zee biplane 10094141; Artis Q floor 10848280; Artis Q biplane 10848282; Artis Q.zen floor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V640000·2019-08-30

    Lion Recalls 2018 Electric School Buses Due to Brake Connector Issue

    Lion Electric Company is recalling 2018 Lion C electric school buses because loose auxiliary brake pump connectors may cause loss of braking ability if the main pump fails.

    Product
    LION — LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V637000·2019-08-29

    Chrysler Recalls 2019-2020 Jeep Cherokee for Steering Rack Gear Defect

    Chrysler is recalling 2019-2020 Jeep Cherokee vehicles because the steering rack gear may break, potentially causing a loss of steering control and increasing crash risk.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V632000·2019-08-29

    Ford Recalls 2013-2016 Fusion, MKZ, Edge, and MKX for Steering Defect

    Ford is recalling 116,160 vehicles because road salt may corrode steering bolts, causing loss of power steering assist and increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD MKZ, EDGE, FUSION, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2226-2019·2019-08-28

    Edwards SAPIEN 3 Ultra Heart Valve System Recalled for Burst Balloons

    Edwards Lifesciences is recalling SAPIEN 3 Ultra Transcatheter Heart Valve Systems due to reports of burst balloons that caused difficulty retrieving the device during procedures.

    Product
    Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (26mm) 9630TF26 UDI:00690103201253
    Category
    Medical Device
    Distribution
    12 states
  • CriticalFDA (Food)·F-2074-2019·2019-08-28

    Kroger Frozen Triple Berry Medley Recalled for Possible Hepatitis A

    The Kroger Co is recalling Private Selection Frozen Triple Berry Medley due to possible Hepatitis A contamination. Consumers should discard the product.

    Product
    PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz
    Category
    Food
    Distribution
    30 states
  • CriticalFDA (Food)·F-2076-2019·2019-08-28

    Kroger Private Selection Frozen Blackberries Recalled for Hepatitis A Risk

    The Kroger Co is recalling 16 oz packages of Private Selection Frozen Blackberries due to possible Hepatitis A contamination. The product was distributed to retail locations in 30 states.

    Product
    PRIVATE SELECTION FROZEN BLACKBERRIES, 16 oz
    Category
    Food
    Distribution
    30 states
  • CriticalFDA (Food)·F-2070-2019·2019-08-28

    Elevation Foods Recalls Archer Farms Egg Salad Due to Listeria

    Elevation Foods is recalling Archer Farms egg salad because Listeria monocytogenes was found in the product. The recall covers 572 cases distributed to multiple states.

    Product
    Archer Farms egg salad packaged in 12oz plastic cup with lid, 6 cups per case, refrigerated
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-2077-2019·2019-08-28

    Kirkland Signature Three Berry Blend Recalled for Hepatitis A Risk

    Townsend Farms Inc. is recalling Kirkland Signature Three Berry Blend frozen berries due to potential Hepatitis A virus contamination.

    Product
    Kirkland Signature Three Berry Blend product, frozen, package in a plastic bag. Net wt. 4 lbs. UPC 0 96619 10105 4. The product label is read in parts: "*** KIRKLAND Signature *** Three Berry Blend *** Raspberries***Blueberries***Blackberries*** PRODUCT OF USA ***…
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-2075-2019·2019-08-28

    Kroger Frozen Triple Berry Medley Recalled for Possible Hepatitis A

    The Kroger Co is recalling Private Selection Frozen Triple Berry Medley due to possible Hepatitis A contamination. Consumers should check their freezers for the affected product.

    Product
    PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 16 oz
    Category
    Food
    Distribution
    30 states
  • CriticalFDA (Food)·F-2090-2019·2019-08-28

    Dole Baby Spinach Recalled Due to Positive Salmonella Test

    Dole Fresh Vegetables is recalling specific lots of Dole Baby Spinach after a Michigan state test detected Salmonella.

    Product
    Dole Baby Spinach: 6 oz. (170 g) plastic bag, UPC 0-71430-00964-2, SKU 320; 10 oz. (283 g) clamshell, UPC 0-71430-00016-8, SKU 2337 Distributed by: Dole Fresh Vegetables, Inc., Monterey, CA 93940.
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-2227-2019·2019-08-28

    Edwards SAPIEN 3 Ultra Heart Valve System Recalled for Burst Balloons

    Edwards Lifesciences is recalling SAPIEN 3 Ultra Transcatheter Heart Valve Systems because burst balloons can make it difficult to remove the device from patients.

    Product
    Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (29mm) 9630TF29 UDI:00690103201260
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Drugs)·D-1843-2019·2019-08-28

    SCA Pharmaceuticals Recalls Ketamine Injection Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 922 syringes of Ketamine 50 mg/5 mL injection due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·19189·2019-08-28

    Whirlpool Recalls Glass Cooktops with Touch Controls Due to Burn and Fire Hazards

    Whirlpool is recalling about 26,300 glass cooktops with touch controls because the surface elements can turn on by themselves, posing burn and fire hazards.

    Product
    Whirlpool, KitchenAid and JennAir brand glass cooktops with touch controls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·087-2019·2019-08-28

    Bakkavor Recalls Chicken Salad for Undeclared Pecans and Misbranding

    Bakkavor Foods USA is recalling 1,913 pounds of ready-to-eat chicken salad products due to undeclared pecans and misbranding. The products were shipped to retail grocery locations in Texas.

    Product
    Bakkavor US - San Antonio — Bakkavor Foods USA, Inc. Recalls Ready-To-Eat Chicken Salad Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V633000·2019-08-28

    Ford Recalls 639,137 Vehicles for Defective Seat Back Recliner Mechanisms

    Ford is recalling 639,137 vehicles because a missing part in the seat back recliner mechanism may reduce strength and fail to restrain occupants in a crash.

    Product
    FORD — FORD, LINCOLN F-150, ESCAPE, F-550, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V634000·2019-08-28

    2020 MINI Cooper and JCW Recalled for Missing Rear Crash Pads

    BMW is recalling 2020 MINI Cooper, Cooper S, and JCW vehicles because rear side trim panels may lack crash pads, increasing injury risk in side impacts.

    Product
    MINI — MINI JCW, COOPER, COOPER S
    Category
    Vehicle
    Distribution
    Distributed nationwide