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.

6126–6150 of 29110

  • SevereNHTSA·22V688000·2022-09-14

    Thomas Built Saf-T-Liner HDX School Buses Recalled for Panel Joint Strength

    Daimler Trucks North America is recalling 2020-2023 Thomas Built Saf-T-Liner HDX school buses because rear side-body panels may have insufficient joint strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    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-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 (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
  • SevereNHTSA·22V683000·2022-09-13

    BMW Recalls 2022 745E Hybrid Vehicles Due to Battery Fire Risk

    BMW is recalling one 2022 745E hybrid vehicle because an improperly sized battery cell electrode may cause a short-circuit and increase the risk of fire.

    Product
    BMW — BMW 745E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V678000·2022-09-12

    Mercedes-Benz Recalls 2022 C 300 Vehicles for Electrical Short Risk

    Mercedes-Benz is recalling 2022 C 300 vehicles because moisture in the trunk may cause an electrical short in the signal acquisition module, increasing the risk of fire or crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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 — WESTERN STAR 49X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V679000·2022-09-12

    Mercedes-Benz Recalls 2021 GLB 250 Vehicles Due to Electrical Fire Risk

    Mercedes-Benz is recalling 2021 GLB 250 vehicles because a damaged Electronic Stability Program unit may cause an electrical short circuit, increasing the risk of fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    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
  • SevereNHTSA·22V675000·2022-09-08

    Ford Recalls 2022 F-150 Raptors Due to Wheel Lug Nut Tightening Issue

    Ford is recalling 2022 F-150 Raptor Series vehicles with 37-inch tires because incorrectly tightened wheel lug nuts may loosen, increasing the risk of wheel separation and a crash.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1638-2022·2022-09-07

    Vegetable Protein Product Recalled for Potential Botulism and Cronobacter

    Lyons Magnus recalls 53,818,025 units of Golden Gloss vegetable protein due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The product was distributed nationwide.

    Product
    Golden Gloss 21837. Item# 20658861 / 30728137.LM2 Ingredients: Water, vegetable protein (pea) and less than 2% of dextrose, maltodextrin, sunflower oil. Net Wt. 34.06 lb (15.45G) Distributed by Kerry Beloit, WI 53511
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1627-2022·2022-09-07

    Milk Chocolate Protein Shake Recalled for Potential Bacterial Contamination

    Lyons Magnus is recalling approximately 53.8 million units of MRE Milk Chocolate Protein Shake nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    MRE Milk Chocolate Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57391 6. 4-count case UPC 810044573947. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487
    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-1607-2022·2022-09-07

    Cold Coffee Recalled Nationwide for Bacterial Contamination Risk

    Intelligentsia Cold Coffee in 10.9 oz containers is recalled nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. Consumers should not consume the product.

    Product
    Intelligentsia, Cold Coffee. Net 10.9 fl oz (325 mL) Tetra Pak container UPC 8 00222-00096 9. Shake Best enjoyed cold. Refrigerate after opening. Produced for: Intelligentsia Coffee, Inc., Aloha, Chicago, IL 60612.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1606-2022·2022-09-07

    Aloha Organic Protein Drink recalled nationwide for potential bacterial contamination

    Lyons Magnus is recalling 53.8 million units of Aloha Organic Protein Drink iced coffee variety nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Aloha Organic Protein Drink, Iced Coffee Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11238 6. Sold as 4 count package wrap with UPC 842096122385. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1610-2022·2022-09-07

    Lyons Ready Care Thickened Dairy Drink recalled for potential pathogen contamination

    Lyons Magnus is recalling Ready Care Thickened Dairy Drink nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Multiple lot codes are affected; consumers should not consume affected product.

    Product
    Lyons Ready Care Thickened Dairy Drink. Mildly Thick Nectar Consistency. Pasteurized - Grade A Made with 2% Milk Fat Milk, Vitamins A & D Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 45796-10043 5. Item 10043. 24 count case UPC 1004579
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1649-2022·2022-09-07

    Cafe Grumpy Cold Brew Coffee Recalled for Potential Bacterial Contamination

    Lyons Magnus is recalling Cafe Grumpy Ready to Drink Cold Brew Coffee nationwide due to findings of and potential for Cronobacter sakazakii and Clostridium botulinum. Affected lots have best-by dates of 08/27/2022 or 08/28/2022.

    Product
    Cafe Grumpy Ready to Drink Cold Brew Coffee 11 fl oz. UPC 7 58524-05908 9. Sold in 4-count case UPC 00758524059003. Refrigerate after opening. Shake before opening. Cafe Grumpy Beverage Company, 199 DiamondSt., Brooklyn, NY 11222
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1605-2022·2022-09-07

    Aloha Organic Protein Drink Recalled for Bacterial Contamination

    Aloha Organic Protein Drink in Vanilla flavor is being recalled nationwide due to findings of Cronobacter sakazakii and Clostridium botulinum. Affected products include specific lot codes with best-by dates from 2022 and 2023.

    Product
    Aloha Organic Protein Drink, Vanilla Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11234 8. Sold in 4 count Package wrap with UPC 842096122347. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1521-2022·2022-09-07

    NIM EMG Endotracheal Tubes recalled for risk of airway obstruction

    Medtronic Xomed is recalling NIM EMG Endotracheal Tubes due to reports of airway obstruction during use. The recall affects 23,820 units distributed worldwide.

    Product
    NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1651-2022·2022-09-07

    Plant-Based Protein Shake Vanilla Recalled for Potential Bacterial Contamination

    Tone It Up Plant-Based Protein Shake Vanilla is being recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Consumers should not consume the product and should contact the distributor.

    Product
    Tone It Up Plant-Based Protein Shake Vanilla. 11 fl oz. UPC 8 10745-03177 7. Sold in 4-count case UPC 00810745032361. Shake Well. Serve Cold. Refrigerate after opening and use within 48 hours. Distributed by Tone It Up, Manhattan Beach, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1657-2022·2022-09-07

    Sated Complete Keto Meal Shake Chocolate recalled for potential bacterial contamination

    Lyons Magnus, Inc. recalls Sated Complete Keto Meal Shake Chocolate Flavor due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. More than 53 million units distributed nationwide.

    Product
    Sated Complete Keto Meal Shake Chocolate Flavor. 11 fl oz (325ml) UPC 8 57227-00721 9. 12 Count Case UPC 00857227007219. Distributed by LongRun LLC, Belmont, MA 02478. Important: Must be refrigerated after opening to maintain safety.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1631-2022·2022-09-07

    Sysco Imperial Dairy Drink Recalled for Cronobacter and Botulism

    Lyons Magnus recalled Sysco Imperial Thickened Dairy Drink nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. The FDA Class I recall affects over 53 million units distributed in 8 oz and 32 oz containers.

    Product
    Sysco Imperial Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Made with Grade A 2% Fat Milk, Vitamins A & D. Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 74865-94550 9. Reorder # 0429357. 24 count case UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1667-2022·2022-09-07

    Kate Farms Nutrition Shake recalled for potential bacterial contamination

    Kate Farms Nutrition Shake (Coffee, 11 fl oz) is being recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects products with lot codes 7331 and 8031.

    Product
    kate farms Nutrition Shake, Coffee. 11 fl oz (325 mL) UPC 8 11112-03062 1. 12 count case UPC 00811112030638. 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
  • SevereFDA (Food)·F-1664-2022·2022-09-07

    Abbott PediaSure Harvest infant nutrition recalled for bacterial contamination

    Abbott PediaSure Harvest 1.0 Cal formula is being recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria.

    Product
    Abbott PediaSure Harvest 1.0 Cal, For Tube Feeding. Complete nutrition blend. 8 fl oz (237mL). UPC 0 70074-67963 1. 24 count case UPC 00070074679624. Shake very well. Store unopened at room temperature. Once opened, reclose, refrigerate, and use within 24 hours. Manufact
    Category
    Food
    Distribution
    Distributed nationwide