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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21251–21275 of 114369

  • SevereFDA (Devices)·Z-2378-2023·2023-08-23

    Dialysis catheter recall: excessive lubricant causes center lumen obstruction

    A dialysis catheter product is being recalled due to excessive lubricant coating in the center lumen, which may cause full or partial obstruction. The blockage could delay treatment and increase risk of blood clots and hemolysis.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, Kit REF: 8888340629
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2369-2023·2023-08-23

    Dialysis Catheter Recalled Due to Silicone Lubricant Obstruction Risk

    Covidien LP is recalling 5,373 MAHURKAR dialysis catheters because excessive silicone lubricant can occlude the catheter lumen, potentially causing treatment delays or blood clotting complications.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, IC Tray REF: 8888101003HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2389-2023·2023-08-23

    MAHURKAR Dialysis Catheter Recalled for Center Lumen Obstruction Risk

    Covidien LP recalled 15,209 MAHURKAR dialysis catheters due to excessive lubricant in the center lumen, which may cause catheter occlusion, reduce blood flow, or lead to hemolysis and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2385-2023·2023-08-23

    Acute Dialysis Catheter Recalled for Potential Lumen Obstruction and Embolism Risk

    Covidien is recalling MAHURKAR acute dialysis catheters for excessive silicone lubricant causing lumen obstruction that may delay treatment and lead to hemolysis, embolism, or thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, Kit REF: 8888345603HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2380-2023·2023-08-23

    FDA Recalls Mahurkar Dialysis Catheter for Potential Tip Obstruction Risk

    Covidien's Mahurkar acute dialysis catheters may have excessive silicone lubricant causing tip obstruction. This could delay treatment or cause serious complications including blood clots and embolism.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, Kit REF: 8888340637
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2384-2023·2023-08-23

    Dialysis catheters recalled for potential center lumen obstruction

    Covidien LP is recalling MAHURKAR dialysis catheters because excessive silicone lubricant coats the center lumen, potentially blocking blood flow or creating clots and other blood vessel complications.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, Kit" REF: 8888345603
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2368-2023·2023-08-23

    Dialysis Catheter Recalled Due to Excessive Lubricant Causing Center Lumen Obstruction

    Covidien is recalling MAHURKAR dialysis catheters due to excessive silicone-based lubricant coating the center lumen tip, which may cause partial or complete obstruction, delaying treatment or causing thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, IC Tray REF: 8888101002HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2375-2023·2023-08-23

    Dialysis catheter recalled due to excessive lubricant causing obstruction

    Covidien's MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can block the center lumen, preventing or reducing blood flow during dialysis. This Class I recall affects 271 units and carries risk of treatment delays, hemolysis, and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, PASS Tray REF: 8888103004HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1443-2023·2023-08-23

    Brain Enhancer Capsules Recalled for Potential E. coli Contamination

    Global Vitality Inc. is recalling Food Research International Serious Brain Enhancer Capsules due to potential E. coli contamination. The product was distributed to a single location in California.

    Product
    Food Research International - Serious Brain Enhancer Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1440-2023·2023-08-23

    Trader Joe's Joe-Joe's Cookies Recalled for Undeclared Peanut Allergen

    Commercial Bakeries is recalling Trader Joe's Joe-Joe's Chocolate Vanilla Creme cookies due to undeclared peanut allergen. Consumers with peanut allergies should not consume this product and should return it to the store.

    Product
    Trader Joe's Joe-Joe's Chocolate Vanilla Creme Flavored With Other Natural Flavors Net Wt.13.4 oz (380g) UPC: 0076 5725 Packaged in trays. 26 units per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2427-2023·2023-08-23

    Endoscopic surgical clamp recalled for potential rotation knob failure

    Carefusion recalls Snowden-Pencer MIS Diamond-Touch Clamps (Lot B23) due to potential cracking of the rotation knob from incorrect adhesive use. The 7 affected units were distributed to the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 45CM, RATCHETED, REF SP90-7243; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2414-2023·2023-08-23

    FreeStyle Libre 2 Readers may fail to activate new sensors

    FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.

    Product
    FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2420-2023·2023-08-23

    Endoscopic surgical clamp recalled for defective rotation knob

    Carefusion 2200 Inc is recalling specific lots of Snowden-Pencer MIS DIAMOND-TOUCH surgical clamps because the rotation knob may crack or break due to a manufacturing defect. Lots B23 and C23 are affected.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 35 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7044; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2426-2023·2023-08-23

    Endoscopic surgical graspers recalled for potential rotation knob failure

    Carefusion is recalling specific lots of Snowden-Pencer surgical graspers used in endoscopy due to a manufacturing defect that could cause the rotation knob to crack or break. The affected instrument may malfunction during surgical procedures.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 45CM, RATCHETED, REF SP90-7220; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1431-2023·2023-08-23

    NatureBest Pre-Cut Lettuce Kits Recalled for Potential Deer Fecal Contamination

    NatureBest Pre-Cut & Produce LLC is recalling salad kits sold in Texas due to potential presence of deer fecal matter. No illnesses have been reported.

    Product
    SALAD KIT-NO COLOR-11CT LETTUCE-4 WAY/MIX-4/5# LETTUCE-ROM/GRN LF 60/40-4/3# LETTUCE-ROMAINE-SHREDDED-4/5# LETTUCE-ROM-1x1-GRN ONLY-6/2# LETTUCE-4 WAY/MIX-2/5# LETTUCE-4 WAY/MIX-1/5# LETTUCE-ROMAINE-CUT-6/2#
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2424-2023·2023-08-23

    Endoscopic surgical grasper recalled due to rotation knob defect

    Carefusion is recalling specific lots of Snowden-Pencer Diamond-Touch endoscopic graspers due to a manufacturing defect that may cause the rotation knob to crack or break. Affected units were distributed in the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 32CM, RATCHETED HANDLE, REF SP90-7066; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1448-2023·2023-08-23

    Frozen Sachertote Recalled for Undeclared Egg, Milk, and Wheat Allergens

    Lidl US TRADING is recalling Alpenfest Style Sachertote frozen dessert because egg, milk, and wheat allergens are not declared on the label. Consumers with allergies to these ingredients should not consume the product.

    Product
    Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2418-2023·2023-08-23

    Endoscopic Dissector Surgical Tool Recalled for Cracking Knob Defect

    Carefusion 2200 Inc is recalling Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR endoscopic surgical instruments due to potential cracking of the rotation knob from incorrect adhesive use in manufacturing. Lot B23 is affected.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR FENESTRATED 16MM JAW 5MM, 32CM, NON RATCHETED, REF SP90-7036; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1405-2023·2023-08-23

    Dilettante Dark Ephemere Bulk Truffles Milk Allergen Mislabeling

    Dilettante Mocha Cafe Dark Ephemere Bulk Truffles' display placard lists milk in ingredients but declares only 'Contains: Dairy,' not 'Contains: Milk.' Bulk boxes have correct allergen labeling.

    Product
    Dilettante Mocha Cafe brand Dark Ephemere Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk, cream, and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1442-2023·2023-08-23

    Uro Kid Support Capsules recalled due to potential E. coli contamination

    Global Vitality Inc. is recalling Uro Kid Support Capsules due to potential E. coli contamination. The affected product was distributed to a single location in California.

    Product
    Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2417-2023·2023-08-23

    Endoscopic surgical graspers recalled for potential rotation knob cracking

    Carefusion is recalling Snowden-Pencer MIS surgical graspers (lot B23) distributed in the US and Canada because the rotation knob may crack or break due to a manufacturing adhesive defect. Affected devices could malfunction during surgical use.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7020; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1429-2023·2023-08-23

    Romaine Lettuce Recalled Due to Potential Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce All American sold in four states due to potential contamination with deer feces.

    Product
    Lettuce Romaine All American, packaged in the following sizes and configurations: 1. Produce Code 476702, 1-5 lb. bag per shipping case, Customer UPC 8398299; 2. Produce Code 476709, 4-5 lb. bags per shipping case, Customer UPC 476709, 8336156, and 8398281.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1423-2023·2023-08-23

    Romaine lettuce recalled due to potential deer feces contamination

    G.O. Corporation is recalling romaine lettuce in multiple package sizes due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, Produce Code 720325, 4-2.5lb. bags per shipping case, Customer UPC 9120457. 2. Romaine Shred 1/4", Produce Code 720425, 4-2.5lb bags per shipping case, Customer UPC 7641269…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1427-2023·2023-08-23

    Romaine Lettuce Recalled Due to Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce 80/20 GB due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lettuce Romaine 80/20 GB, packaged in the following sizes and configurations: 1. Produce Code 448007, 2-5 lb. bags per shipping case, 2. Produce Code 448007, 4-5 lb. bags per shipping case, 3. Produce Code 448110, 4-5 lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1402-2023·2023-08-23

    Trader Joe's Falafel Recalled for Foreign Object Contamination

    Trader Joe's Fully Cooked Falafel Heat & Eat is being recalled from Connecticut, Texas, and Illinois due to the presence of rocks in the product. Consumers should return affected packages to the point of purchase.

    Product
    Trader Joe's Fully Cooked Falafel Heat & Eat NET WT. 12 OZ (340g) Distributed and Sold Exclusively By: Trader Joe's Monrovia, CA 91016 UPC 0093 9355
    Category
    Food
    Distribution
    3 states