The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

3251–3275 of 4878

  • SevereFDA (Drugs)·D-1502-2022·2022-09-21

    FDA Recalls CITROMA Magnesium Citrate for Microbial Contamination

    Vi-Jon, LLC is recalling CITROMA magnesium citrate oral laxative solution due to microbial contamination. The affected product was distributed nationwide in the USA, Canada, and Panama.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1727-2022·2022-09-21

    EZ Noble Sushi Spicy Tuna Roll Recalled for Undeclared Egg Allergen

    EZ Noble Sushi is recalling Spicy Tuna Roll (9.6 oz) with expiration 08/12/2022 due to undeclared egg. Consumers with egg allergies should not consume this product.

    Product
    Spicy tuna roll (9.6 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
  • 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-1505-2022·2022-09-21

    Magnesium Citrate Laxative Recalled Due to Microbial Contamination

    Vi-Jon's Magnesium Citrate oral solution laxative is recalled nationwide due to microbial contamination. Approximately 8,682 bottles are affected.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1726-2022·2022-09-21

    Spicy salmon rolls recalled for undeclared egg allergen

    EZ Noble Sushi recalls spicy salmon rolls (9.6 oz, expiration 08/12/2022) sold in MA and CT due to undeclared egg allergen.

    Product
    Spicy salmon roll (9.6 oz) with expiration 08/12/2022
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0212-2024·2022-09-21

    Banana Boat Clear Sunscreen Spray recalled for benzene contamination

    Edgewell Personal Care Brands is recalling Banana Boat hair & scalp defense Clear Sunscreen Spray SPF 30 due to benzene contamination. The affected product was distributed nationwide in the United States.

    Product
    Banana Boat hair & scalp defense, Clear Sunscreen Spray SPF 30, Avobenzone 2.0%, Homosalate 6.0%, Octocrylene 6.0%, packaged in Net Wt 6 oz. aluminum spray can, Distributed by: Edgewell Personal Care Brands, LLC, Shelton, CT 06484, UPC 0 79656 04041 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1507-2022·2022-09-21

    SWAN Citroma Saline Laxative Recalled for Microbial Contamination

    Vi-Jon is recalling SWAN Citroma Magnesium Citrate Saline Laxative (10 FL OZ bottles) due to microbial contamination of a non-sterile product. The product was distributed nationwide in the USA, Canada, and Panama.

    Product
    SWAN, Citroma MAGNESIUM CITRATE, Saline Laxative, Oral Solution, (1.745 g/fl oz), Lemony Flavor, 10 FL OZ (296 mL), Distributed by: Vi-Jon, Inc. One Swan Drive Smyrna, TN 37167; NDC 0869-0166-38 UPC 0 72785 13405 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1731-2022·2022-09-21

    Shrimp tempura and lobster roll recalled for undeclared wheat allergen

    EZ Noble Sushi is recalling shrimp tempura and lobster roll products with expiration date 08/12/2022 distributed in Massachusetts and Connecticut due to undeclared wheat allergen.

    Product
    Shrimp tempura & lobster roll (12.8 oz) with expiration 08/12/2022
    Category
    Food
    Distribution
    2 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 (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-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
  • 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 (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 (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-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-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 (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
  • 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
  • SevereFDA (Food)·F-1614-2022·2022-09-07

    Lyons Ready Care 2.0 Vanilla Drink Recalled Nationwide for Bacterial Contamination

    Lyons Magnus is recalling Lyons Ready Care 2.0 Vanilla nutritional drink nationwide due to findings and potential for Cronobacter sakazakii and Clostridium botulinum contamination. Consumers should not consume affected products.

    Product
    Lyons Ready Care 2.0 Vanilla High Calorie, High Protein, Nutritional Drink. 32 FL OZ (1 QT) 946mL UPC 0 45796-10091 6 Item 10091. 12 count case UPC 10045796100913. Refrigerate after opening. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1643-2022·2022-09-07

    Stumptown Cold Brew Coffee Recalled Nationwide for Bacterial Contamination

    Lyons Magnus Inc. is recalling Stumptown Cold Brew Coffee with Cream & Sugar nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria.

    Product
    Stumptown Cold Brew Coffee with Cream & Sugar Chocolate. 11 Fl Oz. 325 ML. UPC 8 55186-00686 1. Sold in 12-count case UPC 108551860006861. Manufactured for Stumptown Coffee Roasters, 100 SE Salmon St. Portland, OR 97214
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1658-2022·2022-09-07

    Protein Drink Recalled for Potential Cronobacter and Botulinum Contamination

    Lyons Magnus recalls Rejuvenate Muscle Health+ Vanilla nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Consumers should not consume affected products.

    Product
    Rejuvenate Muscle Health+ Vanilla. 11 fl oz. (330mL) UPC 6 29046-50402 2. Serve Cold, shake well. Manufactured exclusively for Element Nutrition, Ltd., 1887 Whitney Mesa Dr. #6020, Henderson, NV 89014. 4-count Case UPC 629046544028.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1645-2022·2022-09-07

    Lyons Barista Style Soy Non-Dairy Beverage recalled for potential bacterial contamination

    Lyons Magnus is recalling Lyons Barista Style Soy Non-Dairy Beverage nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination affecting over 53 million units.

    Product
    Lyons Barista Style Soy Non-Dairy Beverage. 32 fl oz. (1QT) 946mL UPC 0 45796-10181 4. Sold in 12-count case UPC 10045796101811. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1666-2022·2022-09-07

    Kate Farms Nutrition Formula Recalled for Cronobacter and Botulinum Risk

    Kate Farms Standard nutrition formula in 325 mL bottles is being recalled due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Approximately 53,818,025 units distributed nationwide.

    Product
    kate farms Standard 1.0 Cal/mL, Vanilla, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 51823-00663 8. 12 count case UPC 00851823006683. Shake Well. A ready-to-use oral and tube feeding formula with intact organic pea protein. Made for Kate Farms, Inc., 101 Innovat
    Category
    Food
    Distribution
    Distributed nationwide