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 deaths or serious injuries are reported, 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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4326–4350 of 6147

  • SevereFDA (Drugs)·D-1501-2022·2022-09-21

    Equate Magnesium Citrate Saline Laxative Recalled Due to Microbial Contamination

    Equate Magnesium Citrate saline laxative has been recalled for microbial contamination. The FDA Class I recall affects 18,324 bottles distributed in the US, Canada, and Panama.

    Product
    equate Magnesium Citrate, SALINE LAXATIVE, (1.745g/fl oz) 10 FL OZ (296mL), Grape Flavor, Distributed By: Walmart, Inc. Bentonville, AR 72716; NDC 49035-592-38 UPC 6 81131 28715 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1725-2022·2022-09-21

    Shrimp Tempura Sushi Rolls Recalled for Undeclared Egg and Wheat

    EZ Noble Sushi is recalling Shrimp Tempura and spice shrimp rolls (11.2 oz, expiration 08/12/2022) due to undeclared egg and wheat allergens. Consumers with allergies to eggs or wheat should not consume this product.

    Product
    Shrimp Tempura and spice shrimp roll (11.2 oz) with expiration 08/12/2022
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1510-2022·2022-09-21

    Walgreens Magnesium Citrate Laxative Recalled for Microbial Contamination

    Walgreens Dye-Free Magnesium Citrate Saline Laxative is recalled nationwide due to microbial contamination affecting certain lots. Consumers should stop using the product immediately.

    Product
    Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Grape Flavor, 10 FL OZ (296 mL), Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015; NDC 0363-7162-38 UPC 3 11917 20159 7 (purple label).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V693000·2022-09-15

    2021 Nissan Versa and Kicks power steering sensor defect

    Nissan is recalling 2021 Versa and Kicks vehicles because an intermittent electrical connection in the power steering torque sensor can disable power steering assist, increasing steering effort and crash risk.

    Product
    NISSAN — 2021 NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1690-2022·2022-09-14

    Select Bakery Cheese Streusel Supreme Recalled for Undeclared Walnuts and Food Colorants

    Select Bakery Cheese Streusel Supreme is recalled due to undeclared walnuts and food colorants. Consumers with allergies or sensitivities to walnuts, Yellow #5, Yellow #6, or Red #40 should not consume this product.

    Product
    Select Bakery Cheese Streusel Supreme Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10054 4
    Category
    Food
    Distribution
    3 states
  • CriticalCPSC·22221·2022-09-14

    ThyssenKrupp Residential Elevators Recalled Due to Child Entrapment Hazard

    ThyssenKrupp Access Corp. is recalling about 16,800 residential elevators sold between 1996 and 2012 due to an entrapment hazard. Children can become trapped in the gap between exterior and interior doors, resulting in serious injury or death; one child death has been reported.

    Product
    thyssenkrupp Access Corp. Residential Elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1476-2022·2022-09-14

    Milk of Magnesia Recalled Nationwide for Microbial Contamination

    Plastikon Healthcare LLC has recalled Milk of Magnesia USP nationwide due to microbial contamination in non-sterile products. The affected lot (20071A) included approximately 24,400 institutional-use cups.

    Product
    MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6846-73.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1657-2022·2022-09-14

    Philips OmniLab Advanced+ sleep apnea devices recalled for off-gassing

    Philips Respironics is recalling 85 units of the OmniLab Advanced+ ventilation device due to motor assemblies containing nonconforming plastic that off-gasses volatile organic compounds.

    Product
    Philips OmniLab Advanced+, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-1658-2022·2022-09-14

    Philips OmniLab Advanced+ Ventilation Devices Recalled for Plastic Off-Gassing

    Philips Respironics is recalling certain Philips OmniLab Advanced+ noninvasive ventilation devices due to motor assemblies with nonconforming plastic that can off-gas volatile organic compounds (VOCs). This is an FDA Class I recall.

    Product
    Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-1656-2022·2022-09-14

    Philips BiPAP V30 Auto Respirators Recalled for VOC Off-Gassing Risk

    Philips Respironics recalls 295 BiPAP V30 Auto respiratory devices due to motor assemblies with nonconforming plastic. These assemblies off-gas volatile organic compounds (VOCs) during device operation.

    Product
    Philips BiPAP V30 Auto, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-1654-2022·2022-09-14

    Philips BiPAP A30 respiratory device motor assemblies recalled for VOC off-gassing

    Philips Respironics recalls Philips BiPAP A30 respiratory devices due to motor assemblies with nonconforming plastic that off-gases volatile organic compounds (VOCs). Patients should contact the manufacturer immediately.

    Product
    Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Drugs)·D-1479-2022·2022-09-14

    Antacid Oral Suspension Recalled Nationwide for Microbial Contamination

    Plastikon Healthcare LLC is recalling an antacid oral suspension distributed nationwide due to microbial contamination. Affected lots 20051A (exp. Aug. 2022) and 20088A (exp. Sep. 2022) should not be used.

    Product
    Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone 240 mg MAX, per 30 mL Oral Suspension, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1655-2022·2022-09-14

    Philips BiPAP A40 Respiratory Devices Recalled for Motor Assembly Off-Gassing

    Philips is recalling BiPAP A40 respiratory support devices because motor assemblies were manufactured with nonconforming plastic that off-gases volatile organic compounds (VOCs). Approximately 1,414 units have been distributed domestically and internationally.

    Product
    Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Drugs)·D-1477-2022·2022-09-14

    Milk of Magnesia USP Recalled for Microbial Contamination Nationwide

    Plastikon Healthcare LLC is recalling Milk of Magnesia USP due to microbial contamination in non-sterile products. Lot 20074A, distributed nationwide for institutional use, should not be used.

    Product
    MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6840-72.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1478-2022·2022-09-14

    Antacid Medication Recalled Nationwide for Microbial Contamination Risk

    Plastikon Healthcare LLC is recalling 220,500 cups of antacid containing magnesium hydroxide and aluminum hydroxide due to microbial contamination.

    Product
    Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1691-2022·2022-09-14

    Select Bakery Brownie Recall: Undeclared Walnuts and Red #40

    Select Bakery Chocolate Chip Brownies (3 oz) are recalled due to undeclared walnuts and Red #40. Product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery CHOCOLATE CHIP BROWNIE Net Wt. 3 Oz (85g) Contains: Wheat, Milk, Soy and Egg ingredients. Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10025 4
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1659-2022·2022-09-14

    Philips OmniLab ventilator recalled for motor assembly plastic off-gassing defect

    Philips Respironics is recalling OmniLab Advanced + ventilators due to motor assemblies manufactured with nonconforming plastic that releases volatile organic compounds (VOCs). The 8 affected units were distributed across the US and internationally.

    Product
    Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereNHTSA·22V681000·2022-09-12

    Commercial Trucks Recalled for Steering Shaft Component Failure

    Daimler Trucks North America is recalling 2022-2023 Western Star 47X and 49X commercial trucks because the steering shaft's u-joint pinch bolt may detach, causing loss of steering control.

    Product
    WESTERN STAR — 2022 WESTERN STAR 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22771·2022-09-08

    Murphy Beds Recalled Due to Serious Impact and Crush Hazards

    Murphy beds sold under Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan brand names can break or detach from walls and fall, posing crush and impact hazards. The manufacturer has received 146 reports of failures with 62 injuries.

    Product
    Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan branded Murphy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1585-2022·2022-09-07

    IQF Frozen Dill Recalled for Listeria Monocytogenes Contamination

    Supherb Farms is recalling IQF Fresh Frozen Dill nationwide and in Canada after testing detected Listeria Monocytogenes in the product. The recall affects approximately 25,009 pounds distributed in 35-pound bulk cases.

    Product
    IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock, CA Perishable, Keep Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1668-2022·2022-09-07

    Kate Farms Nutrition Shake recalled for bacterial contamination nationwide

    Lyons Magnus is recalling Kate Farms Nutrition Shake, Chocolate nationwide due to findings and potential for Cronobacter sakazakii and Clostridium botulinum contamination.

    Product
    kate farms Nutrition Shake, Chocolate. 11 fl oz (325 mL) UPC 8 11112-03060 7. 12 count case UPC 00811112030614. Shake Well. After opening, refrigerate and use within 4 days. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 93708
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1636-2022·2022-09-07

    Lactation Smoothie Recalled Nationwide Due to Bacterial Contamination

    Sweetie Pie Organics Lactation Smoothie is recalled nationwide due to contamination with Cronobacter sakazakii and Clostridium botulinum. Consumers should not consume affected products.

    Product
    Sweetie Pie Organics Lactation Smoothie Apple Pear. 11.1 FL OZ (330 mL) UPC 8 56334-00254 4. No. 975001. Packaged in the following configurations: 1. 12 count case 2. 4 count wrap UPC 856334002575. Refrigerate after opening and consume within 24 hours. Distri
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1635-2022·2022-09-07

    Lactation Smoothie Recalled Nationwide for Potential Bacterial Contamination

    Sweetie Pie Organics Lactation Smoothie Mango Banana is recalled due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 53,818,025 units distributed nationwide.

    Product
    Sweetie Pie Organics Lactation Smoothie Mango Banana. 32 FL OZ (1 QT) 946mL UPC 8 56334-00278 0. No. 955001. Packaged in the following configurations: 1. 12 count case 2. 4 count wrap UPC 856334002810. Refrigerate after opening and consume within 24 hours. Distr
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1611-2022·2022-09-07

    Lyons Ready Care 2.0 Chocolate Drink Recalled for Potential Bacterial Contamination

    Lyons Magnus recalls Lyons Ready Care 2.0 Chocolate Nutritional Drink nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected units have lot codes 8212 and 9302.

    Product
    Lyons Ready Care 2.0 Chocolate High Calorie, High Protein, Nutritional Drink. 32 FL OZ (1 QT) 946mL UPC 0 45796-10050 3 Item 10050. 12 count case UPC 10045796100500. Refrigerate after opening. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1648-2022·2022-09-07

    Lyons Plant-Based Protein Shake Recalled for Bacterial Contamination

    Lyons Magnus is recalling Lyons Ready Care Plant-Based Protein Shake Chocolate nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum, serious bacterial pathogens that can cause illness.

    Product
    Lyons Ready Care Plant-Based Protein Shake Chocolate. 8.45 fl oz. (250mL) UPC 0 45796-10081 7. Mildly Thick Nectar Consistency. Refrigerate prior to serving. Shake Well. Sold in 24-count case UPC 10045796100814. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide