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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

4751–4775 of 6575

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 (Drugs)·D-1503-2022·2022-09-21
FDA Recalls Kroger Magnesium Citrate Laxative for Microbial Contamination
Kroger-branded Magnesium Citrate saline laxative is being recalled due to microbial contamination. The recall affects approximately 44,976 bottles distributed in the USA, Canada, and Panama.
Product
MAGNESIUM CITRATE — MAGNESIUM CITRATE (MAGNESIUM CITRATE)
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-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-1730-2022·2022-09-21
EZ Noble Sushi Rolls Recalled for Undeclared Egg Allergen
EZ Noble Sushi is recalling Pink Lady and Salmon Avocado rolls (9 oz, expiration 08/12/2022) distributed in MA and CT due to undeclared egg. Consumers with egg allergies should not consume this product.
Product
Pink lady and salmon avocado roll (9 oz) with expiration 08/12/2022
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-1508-2022·2022-09-21
OTC Magnesium Citrate Laxative Recalled for Microbial Contamination
Vi-Jon's CITROMA magnesium citrate laxative is recalled due to microbial contamination. Approximately 18,588 bottles were distributed nationwide in the USA, Canada, and Panama.
Product
CITROMA — CITROMA (MAGESIUM CITRATE)
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-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-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-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 (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-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 (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 (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
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-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-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

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