The Recall Desk

Archive

May 2022 recalls

426 recalls were announced in May 2022.

What the numbers show

Critical
12
Severe
68
High
275
Moderate
69
Low
2

Of the 426 recalls this month scored against our rubric, 3% are Critical, 16% are Severe.

201–300 of 426

  • SevereNHTSA·22E039000·2022-05-16

    Carparts.com Recalls Oil Filter Housings Due to Leak and Fire Risk

    Carparts.com is recalling specific oil filter housings because a seal defect may cause oil leaks, increasing the risk of fire or engine failure.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION:FILTER/SCREEN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V340000·2022-05-16

    FCCC MT50E Vans Recalled for Shift Knob Malfunction

    Daimler Trucks North America is recalling 2021-2022 FCCC MT50E walk-in vans because a faulty shift knob may cause unintended movement.

    Product
    FCCC — FCCC MT50E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V339000·2022-05-16

    2022 Freightliner Cascadia trucks recalled for disabled antilock brakes and stability control

    Daimler Trucks North America is recalling approximately 17 certain 2022 Freightliner Cascadia trucks because the antilock brakes and electronic stability control can be manually disabled, violating federal safety standards and increasing crash risk. The company will repurchase affected vehicles.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V338000·2022-05-16

    Commercial trucks recalled for incorrect gross axle weight labels

    Daimler Trucks is recalling commercial trucks with incorrect weight-rating labels that could allow unsafe overloading. Dealers will replace the labels free of charge.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4900, 4700, 5700, NEW CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V341000·2022-05-16

    Utilimaster Walk-in Van Recall for Incorrect Tire Placard Information

    Shyft Group is recalling 2022 Utilimaster Walk-in vans because tire size and pressure labels may be incorrect, potentially leading to improper tire inflation.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V342000·2022-05-16

    Bowlus Endless Highways Travel Trailers Recalled for Gas Leak Risk

    Bowlus is recalling 2022 Endless Highways travel trailers because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    BOWLUS — BOWLUS ENDLESS HIGHWAYS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V337000·2022-05-13

    Ford Recalls 2016 Super Duty Trucks for Air Bag Defect

    Ford is recalling 2016 Super Duty trucks because dust in the steering wheel clock spring may prevent the driver's air bag from deploying.

    Product
    FORD — FORD F-350 SD, F-550 SD, F-450 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V333000·2022-05-13

    Ford Recalls 2021 Mustang Mach-E Vehicles for Software Defect

    Ford is recalling 2021 Mustang Mach-E all-wheel drive vehicles because a software error may cause unintended acceleration or loss of power.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V330000·2022-05-13

    Blue Bird Recalls 2023 Vision Transit Bus for Software Defect

    Blue Bird is recalling one 2023 Vision transit bus because incorrect software settings allow the engine to start while in gear, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-05132022-01·2022-05-13

    Weis Markets Recalls General Tso Chicken Meals Due to Undeclared Milk

    Weis Markets is recalling ready-to-eat General Tso Chicken meals sold in seven states because they may contain undeclared milk, a known allergen.

    Product
    FSIS Issues Public Health Alert for Weis Markets’ Ready-To-Eat General Tso Chicken Meals Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·22V334000·2022-05-13

    2022 Ford Mustang camera misalignment disables forward collision avoidance

    Ford is recalling certain 2022 Mustang vehicles with misaligned front-facing cameras that disable forward collision avoidance and other safety features. Owners should contact Ford customer service at 1-866-436-7332 to schedule free camera realignment.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E038000·2022-05-13

    Plastic Omnium Fuel Tank Assembly Recall for Engine Stall Risk

    Plastic Omnium is recalling fuel tank assemblies used in Nissan and Mitsubishi vehicles because the fuel pump may fail, potentially causing an engine stall and increasing crash risk.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V331000·2022-05-13

    2020 Ford Escape High Voltage Battery Weld Defect Recall

    Ford is recalling certain 2020 Escape and 2021 Corsair hybrid vehicles due to insufficient welds in the high voltage battery that may fail, causing loss of drive power and increased crash risk.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V327000·2022-05-12

    2022 Jeep Grand Cherokee Recall for Hazard Light Flashing Defect

    Chrysler is recalling 2022 Jeep Grand Cherokee vehicles because hazard lights may flash when the brake pedal is applied, potentially confusing other drivers.

    Product
    JEEP — JEEP GRAND CHEROKEE 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V326000·2022-05-12

    2022 Jeep Wrangler Vehicles Recalled for Faulty Side Marker Lights

    Chrysler is recalling certain 2022 Jeep Wrangler vehicles with nonfunctional side marker lights. The defect may reduce vehicle visibility to other drivers, increasing the risk of a crash.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22747·2022-05-12

    Yamaha Wolverine RMAX Off-Road Vehicles Recalled for Fire and Explosion Hazards

    Yamaha is recalling about 4,130 Wolverine RMAX off-road side-by-side vehicles due to damaged fuel tanks that can leak fuel, creating fire and explosion risks. No injuries have been reported to date.

    Product
    Off-Road Side-by-Side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1044-2022·2022-05-11

    TOP SAVOR Licorice Flavored Olive Recalled for Undeclared Sulfites

    A & C Best Food Trading is recalling TOP SAVOR Licorice Flavored Olive products for containing undeclared sulfites. The recalled item was distributed across 12 U.S. states.

    Product
    Olive; TOP SAVOR Licorice Flavored Olive; Net wt: 500g (17.63oz); Ingredients: olive, sugar, salt, licorice extract, food additives (citric acid, saccharin sodium, sodium benzoate, potassium sorbate), edible spices; Store in a cool and dry place. Away from direct sunlight. Distri
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1046-2022·2022-05-11

    Pickled Plums Recalled for Undeclared Sulfites and Prohibited Food Dye

    A & C Best Food Trading is recalling Wife Plum pickled plums in 500g jars for containing undeclared sulfites and prohibited Amaranth dye. The product poses serious health risks to sulfite-sensitive consumers.

    Product
    BEAUTIFUL AND DELICIOUS TASTE; TOP SAVOR; Wife Plum; Net wt. 500g (17.63oz); Ingredients: plum (grafting); sugar, salt, food additives (citric acid, DL malic acid, stevioside, sodium saccharine, potassium sorbate, sodium benzoate), edible spices.; Distributed by A & C best food t
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-1068-2022·2022-05-11

    Salsa Texan tortillas recalled for undeclared wheat and whey allergens

    The Salsa Texan tortillas (coconut flour and blended flour varieties) are being recalled for potentially containing undeclared wheat and whey. Products were distributed online and at farmers markets.

    Product
    The Salsa Texan Coconut Flour Tortilla regular and burrito size packaged in clear flexible plastic; The Salsa Texan Blended Flour Tortilla regular and burrito size packaged in clear flexible plastic; Unlabeled tortillas sold at farmer's market in Dallas, TX area
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0876-2022·2022-05-11

    Hand Sanitizer Product Recalled for Methanol Chemical Contamination

    Mickey Mouse Hand Sanitizer (ethyl alcohol 68%, 2.11 oz. bottles) is being recalled nationwide by Best Brands Consumer Products, Inc. due to methanol contamination in Lot #20D21 (expiration 06/30/2022).

    Product
    Mickey Mouse Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./to mL bottle, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-013-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0944-2022·2022-05-11

    COVID-19 Rapid Test Kits Recalled for Lacking FDA Authorization

    SML Distribution is recalling 209,450 units of Skippack COVID-19 rapid test kits that were distributed without FDA authorization or clearance. The kits were distributed nationwide across Alabama, Florida, Georgia, Missouri, New York, Texas, and Wyoming.

    Product
    Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1043-2022·2022-05-11

    Whole Foods red lentil dal recalled for possible Listeria contamination

    Whole Foods Market red lentil dal (12 oz) may contain Listeria monocytogenes. The affected product was distributed to nine states. Consumers should not consume the product.

    Product
    WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOODS MARKET AUSTIN, TX 78703 UPC 1 95515 02394 8
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·22V325000·2022-05-11

    Beta USA Recalls 2022 RR-S Motorcycles Due to Front Brake Hose Defect

    Beta USA is recalling 2022 350, 390, 430, and 500 RR-S motorcycles because an incorrect front brake hose was installed, which may disconnect and cause a loss of braking.

    Product
    BETA — BETA 350 RR-S, 390 RR-S, 430 RR-S, 500 RR-S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0877-2022·2022-05-11

    The Mandalorian Hand Sanitizer Recalled Nationwide for Benzene Contamination

    The Mandalorian Hand Sanitizer has been recalled nationwide due to FDA-detected benzene contamination. The recall affects 346,320 bottles with lot number 20E21.

    Product
    The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-012-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1021-2022·2022-05-11

    In Vitro Diagnostic Estradiol Test Recalled for Falsely Elevated Results

    Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol (eE2) 500T diagnostic kits that produce falsely elevated test results in plasma specimens, which could lead clinicians to misinterpret patient results.

    Product
    Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995562 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0886-2022·2022-05-11

    Azurion Medical Imaging System Software Defect Alters Dose Parameters

    A software defect in Philips Azurion imaging systems causes the Patient Type to change unexpectedly during study initiation, altering dose control parameters without operator notification.

    Product
    Azurion systems with software release R1.x
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V324000·2022-05-11

    2022 Hyundai IONIQ 5 Parking Brake Software Defect Recall

    Hyundai is recalling certain 2022 IONIQ 5 vehicles due to a software error in the Shifter Control Unit that may disengage the parking brake, allowing the vehicle to rollaway and increasing the risk of a crash.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0853-2022·2022-05-11

    Lansoprazole Tablets Recalled Due to Failed Dissolution Specifications

    Dr. Reddy's Laboratories is recalling Lansoprazole 30 mg orally disintegrating tablets (Lot T2000645) because they failed dissolution specifications. The tablets may not dissolve properly, affecting medication effectiveness.

    Product
    LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-1045-2022·2022-05-11

    Olive King Olives Recalled Due to Undeclared Sulfites

    A & C Best Food Trading is recalling Olive King Olives (14 oz) because they contain undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.

    Product
    Olive King Olives; 14 oz; packaged in clear and green plastic packaging; Ingredients: dried fruit, sugar, salt; Shelf life: 12 months; Product of china
    Category
    Food
    Distribution
    12 states
  • HighFDA (Drugs)·D-0844-2022·2022-05-11

    Alprazolam XR Extended-Release Tablets Recalled Due to Dissolution Failure

    Viatris Inc. is recalling alprazolam XR 3mg tablets (lot EH8348) distributed nationwide due to failed dissolution testing. Tablets may not dissolve properly, potentially reducing drug effectiveness.

    Product
    ALPRAZOLAM — ALPRAZOLAM (ALPRAZOLAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0832-2022·2022-05-11

    Losartan Potassium Tablets Recalled Due to AZIDO Impurity Above Limits

    Macleods Pharma USA Inc. is recalling Losartan Potassium 25 mg tablets due to higher-than-acceptable levels of AZIDO impurity from manufacturing deviations. The affected lots were distributed nationwide.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-051122-01·2022-05-11

    USDA Issues Public Health Alert for Organic Ground Beef Due to Plastic Contamination

    USDA FSIS issued a public health alert for specific Organic Rancher ground beef products due to potential hard plastic contamination. No illnesses have been reported.

    Product
    NPC Processing, LLC — FSIS Issues Public Health Alert for Raw Ground Beef Products Due to Foreign Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0839-2022·2022-05-11

    Losartan Potassium Tablets Recalled Due to Unacceptable Chemical Impurity Levels

    Lupin Pharmaceuticals is recalling 1.47 million bottles of Losartan Potassium Tablets due to chemical impurities exceeding acceptable limits. The affected batches were distributed nationwide.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1038-2022·2022-05-11

    Elegant Foods Macarons Recalled for Undeclared Food Color Additives

    Elegant Foods has recalled 27 cases of Passion Fruit Mango Macarons due to undeclared food color additives including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40. The product was distributed in Wisconsin.

    Product
    elegant foods Passion Fruit Mango Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0850-2022·2022-05-11

    Betamethasone Dipropionate Ointment 0.05% recalled for manufacturing compliance failures

    McKesson Corporation is recalling 55,440 tubes of Betamethasone Dipropionate Ointment 0.05% (Augmented) nationwide due to manufacturing compliance deviations. The recall stems from the manufacturer's discontinuation of its stability study program.

    Product
    Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented) (Potency expressed as betamethasone), 15 gram tube, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 381
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0838-2022·2022-05-11

    Losartan Potassium tablets recalled for AZIDO impurity above limits

    Lupin Pharmaceuticals recalls Losartan Potassium tablets for CGMP deviations with AZIDO impurity above limits. The recall affects 657,336 bottles distributed nationwide; no illnesses reported.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0841-2022·2022-05-11

    Losartan Potassium and Hydrochlorothiazide tablets recalled for AZIDO impurity

    Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide tablets distributed nationwide due to elevated AZIDO impurity levels detected during manufacturing quality control.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1024-2022·2022-05-11

    Siemens ADVIA Centaur Estradiol Test Recalled for Falsely Elevated Results

    Siemens Healthcare is recalling all lots of the ADVIA Centaur Enhanced Estradiol diagnostic test because plasma specimens can produce falsely elevated results, potentially leading clinicians to misinterpret patient results.

    Product
    ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10491445 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1035-2022·2022-05-11

    K-Wire Devices Recalled for Incorrect Length and Diameter Specifications

    Arthrex is recalling 300 K-Wire orthopedic devices that do not meet specified length and diameter requirements. Incorrect dimensions may affect surgical function.

    Product
    K-Wire, 1.35 mm x 170 mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1025-2022·2022-05-11

    Estradiol Diagnostic Device Recalled for Falsely Elevated Test Results

    An estradiol diagnostic device has been recalled because it produces falsely elevated test results in plasma specimens. These inaccurate results could cause clinicians to misinterpret patient test results.

    Product
    ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1027-2022·2022-05-11

    Evans Wedge Disposable Trials Orthopedic Surgical Instruments Recalled for Mixed Parts

    restor3d Inc. is recalling Evans Wedge Disposable Trials orthopedic surgical instruments because parts were mixed into other lots during relabeling for extended shelf-life. The recall affects devices distributed nationwide across seven states.

    Product
    Evans Wedge Disposable Trials, Medium Footprint, 10mm Thickness (6101-20181018). Orthopedic manual surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1034-2022·2022-05-11

    Ultrasonic Gastrovideoscope Recalled Due to Reprocessing Incompatibility and Infection Control Risk

    Olympus recalls the GF-UC140P-AL5 ultrasonic gastrovideoscope nationwide because it is no longer compatible with the OER-Pro reprocessing system, creating an infection control risk to patients.

    Product
    Ultrasonic Gastrovideoscope, GF-UC140P-AL5. Intended for endoscopic real-time ultrasound imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1018-2022·2022-05-11

    Medical Device Software Update Overwrites Custom Antibiotic Codes

    BD Synapsys Microbiology Informatics Software version 4.10 overwrites customer-configured antibiotic codes with BD defaults during system updates, affecting data integrity in clinical microbiology reporting.

    Product
    BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2022·2022-05-11

    Restrata Medical Device Recall: Misprinted Expiration Date on Shelf-Box Packaging

    Acera Surgical Inc is recalling 83 units of the Restrata RWM1-2X2 medical device (Lot Number 51745) due to a misprinted expiration date on the shelf-box packaging distributed nationwide.

    Product
    Restrata, Part Number RWM1-2X2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1028-2022·2022-05-11

    Evans Wedge Orthopedic Surgical Instrument Recalled for Parts Mixed During Rework

    restor3d Inc. is recalling 9 units of Evans Wedge Disposable Trials orthopedic surgical instruments because parts from different lots were mixed during a manufacturing rework and relabeling process.

    Product
    Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness (Model: 6101-22200818). Orthopedic manual surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1031-2022·2022-05-11

    First Aid Kits Recalled Due to Defective Acetaminophen

    ASO LLC is recalling approximately 73,668 first aid kits sold under Equate, Meijer, and Care Science brands that contain previously recalled acetaminophen. Affected kits were distributed nationwide.

    Product
    First Aid Kits containing acetaminophen under brand names Equate (Walmart), Meijer, and Care Science (Amazon)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1020-2022·2022-05-11

    Estradiol diagnostic test kits recalled for falsely elevated results

    Siemens Atellica IM Enhanced Estradiol test kits can produce falsely elevated results in plasma specimens, potentially leading to misinterpretation of patient hormone measurements. Approximately 2,044 units worldwide are affected.

    Product
    Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V321000·2022-05-11

    Blue Bird Recalls 2023 Vision School Buses Due to Software Defect

    Blue Bird is recalling 2023 Vision school buses with Allison transmissions because incorrect software allows the engine to start while in gear, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1023-2022·2022-05-11

    Medical Diagnostic Test Kit Issues Falsely Elevated Estradiol Results

    Siemens Healthcare is recalling ADVIA Centaur Enhanced Estradiol diagnostic kits because plasma specimens may show falsely elevated results, potentially leading clinicians to misinterpret patient test results.

    Product
    ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10490889 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1039-2022·2022-05-11

    Elegant Foods Raspberry Macaron Recalled for Undeclared Food Colorants

    Elegant Foods is recalling Raspberry Macarons because the product contains undeclared artificial food colorants including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.

    Product
    elegant foods Raspberry Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·22V322000·2022-05-11

    2022 KIA EV6 Parking Brake Software Defect May Cause Vehicle Rollaway

    Kia Motors America is recalling 2022 EV6 vehicles due to a software error in the Shifter Control Unit that may disengage the parking mechanism, allowing the vehicle to roll away unexpectedly.

    Product
    KIA — KIA EV6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0843-2022·2022-05-11

    Losartan Potassium and Hydrochlorothiazide tablets recalled for AZIDO impurity

    Lupin Pharmaceuticals recalls Losartan Potassium and Hydrochlorothiazide tablets nationwide due to manufacturing deviations that resulted in AZIDO impurity levels above acceptable limits.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0833-2022·2022-05-11

    Losartan Potassium Tablets Recalled for Manufacturing Impurity Above Acceptable Limits

    Macleods Pharma USA is recalling Losartan Potassium 50 mg tablets nationwide due to CGMP deviations with AZIDO impurity levels above acceptable limits. Affected lots: BLI2002A, BLI2004A, and BLI2104B.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0840-2022·2022-05-11

    Losartan Potassium tablets recalled for manufacturing impurity above limits

    Lupin Pharmaceuticals is recalling Losartan Potassium Tablets 100 mg nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits. Approximately 1,247,067 bottles were affected.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1033-2022·2022-05-11

    Elegant Foods Door County Cherry Macarons Recalled for Undeclared Food Coloring

    Elegant Foods recalls Door County Cherry Macaron (63 cases, Wisconsin) for undeclared artificial food colorants including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.

    Product
    elegant foods Door County Cherry Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0848-2022·2022-05-11

    Lidocaine Hydrochloride Topical Solution Recalled for Manufacturing Quality Deviations

    McKesson Corporation is recalling Lidocaine Hydrochloride Topical Solution due to manufacturing deviations related to discontinuation of the stability study program. Approximately 81,757 bottles distributed nationwide are affected.

    Product
    Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL bottle, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4071 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-977-64
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0834-2022·2022-05-11

    Losartan Potassium Tablets Recalled for Excessive Azido Impurity

    Macleods Pharma is recalling Losartan Potassium Tablets due to CGMP deviations with azido impurity levels exceeding acceptable limits. The recall affects 5.6 million tablets distributed nationwide.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V323000·2022-05-11

    Nova Bus Recalls LFS and LFS Artic Buses Due to Signal Confusion

    Nova Bus is recalling 2016-2020 LFS and 2013-2022 LFS Artic buses because a text message board duplicates stop and turn signals, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0835-2022·2022-05-11

    Losartan potassium and hydrochlorothiazide tablets recalled for manufacturing quality deviations

    Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to manufacturing quality issues with chemical impurity levels above acceptable limits. Affected lots were distributed nationwide in 30-, 90-, and 1000-count bottles.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0836-2022·2022-05-11

    Losartan Potassium and Hydrochlorothiazide Tablets Recalled for Manufacturing Defect

    Macleods Pharma USA Inc is recalling multiple lots of Losartan Potassium and Hydrochlorothiazide tablets (NDC# 33342-052-07, 33342-052-10, 33342-052-44) distributed nationwide due to AZIDO impurity levels exceeding acceptable limits.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0847-2022·2022-05-11

    Halobetasol Propionate Ointment 0.05% Recalled Due to Manufacturing Practice Deviations

    McKesson Corporation is recalling Halobetasol Propionate Ointment 0.05% nationwide after the manufacturer discontinued its stability study program, creating CGMP deviations. Over 13,200 tubes distributed in the United States, Guam, and the Northern Mariana Islands are affected.

    Product
    Halobetasol Propionate Ointment 0.05% Net Wt., 50 gram tube, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging 4071 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-998-67
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0849-2022·2022-05-11

    FDA Recalls Lidocaine Prilocaine Cream Due to Manufacturing Compliance Issue

    McKesson Corporation has recalled Lidocaine Prilocaine Cream 2.5%/2.5% because the manufacturer, Teligent Pharma, Inc., discontinued its stability study program, a deviation from manufacturing standards.

    Product
    Lidocaine Prilocaine Cream USP, 2.5%/2.5% Net Wt. 30 gram tube, Rx Only, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141 Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, NDC 63739-054-66
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1019-2022·2022-05-11

    Baxter Flo-Thru Intraluminal Shunt Recall for Potential Foreign Matter

    Baxter Healthcare is recalling Flo-Thru Intraluminal Shunts due to potential foreign matter contamination. The recall involves 300 devices distributed in the U.S. and internationally.

    Product
    Flo-Thru Intraluminal Shunt. Used in coronary artery or peripheral vascular procedures. Used to shunt blood at the anastomosis to provide a temporary blood-free operative field for suturing while allowing blood to flow distal to the anastomosis.
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-1033-2022·2022-05-11

    Johnson & Johnson Tray Ring Covers Recalled for Sterility Barrier Breach

    Johnson & Johnson Surgical Vision is recalling tray ring covers (Model OM271000) worldwide due to a potential breach in the sterility barrier that could allow contamination.

    Product
    TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2022·2022-05-11

    Estradiol Diagnostic Test Recall: Risk of Falsely Elevated Results

    Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol diagnostic test kits (all lots) due to falsely elevated results in plasma specimens. These inaccurate results could lead clinicians to misinterpret patient data.

    Product
    Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 11206250 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1029-2022·2022-05-11

    Robotic-Assisted Medical Device Recalled Due to Software Defect

    The FDA is recalling the VELYS Robotic-Assisted Solution Base due to a software defect in version 1.5.1 related to Daylight Saving Time changes. The defect can cause system errors requiring restart, potentially delaying patient treatment.

    Product
    VELYS Robotic-Assisted Solution Base Product No.: 451570100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0829-2022·2022-05-11

    Norepinephrine Injection Recalled Nationwide for Manufacturing Quality Deviations

    SCA Pharmaceuticals recalled 120 bags of Norepinephrine 8mg injection nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall was initiated April 25, 2022.

    Product
    Norepinephrine 8mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-078-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1041-2022·2022-05-11

    Elegant Foods Macarons Recalled for Undeclared Food Colorants

    Elegant Foods, LLC is recalling Macaron Variety B due to undeclared food colorants on the label. The product contains six FD&C dyes not listed in the ingredient declaration.

    Product
    elegant foods Macaron Variety B, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1037-2022·2022-05-11

    Elegant Foods Mint Macaron Recall for Undeclared Food Colorings

    Elegant Foods is recalling Mint Macaron products due to missing label declarations for six artificial food colorings. Consumers should stop consumption and return affected products.

    Product
    elegant foods Mint Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1034-2022·2022-05-11

    Elegant Foods Eggnog Macaron Cases Recalled for Undeclared Food Colors

    Elegant Foods is recalling eggnog macaron cases because the packaging fails to disclose food color additives including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.

    Product
    elegant foods Eggnog Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0851-2022·2022-05-11

    Erythromycin Topical Gel Recalled Due to Manufacturing Quality Deviations

    McKesson Corporation is recalling Erythromycin Topical Gel USP 2% due to CGMP deviations. The manufacturer discontinued its stability study program, prompting a nationwide recall of all products within their expiration date.

    Product
    Erythromycin Topical Gel USP, 2%, Net Wt 60 g tube, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-053-68
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0842-2022·2022-05-11

    Losartan Potassium and Hydrochlorothiazide Tablets Recalled for Impurity

    Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets nationwide due to AZIDO impurity levels above acceptable limits. Patients should consult their healthcare provider about their medication.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0830-2022·2022-05-11

    Drug recall: fentanyl and bupivacaine injectable solution manufacturing deviations

    SCA Pharmaceuticals voluntarily recalled 424 bags of fentanyl and bupivacaine injectable solution due to manufacturing control deviations. The product was distributed nationwide in the United States.

    Product
    Fentanyl 2mcg/ml and Bupivacaine 0.125% in 0.9% Sodium Chloride 100 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0231-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1026-2022·2022-05-11

    Cervical Cage Trial Kit Recalled for Incorrect Size Labeling

    restor3d Inc. is recalling 14 units of its Non-Sterile Double Ended Trial Kit because the product was labeled as Small Footprint when it is actually Medium. The lot was distributed nationwide across seven states.

    Product
    Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1032-2022·2022-05-11

    Elegant Foods Lemon Macarons Recalled for Undeclared Food Color Additives

    Elegant Foods is recalling Lemon Macarons (Code 213645A) because the product contains six food color additives that are not declared on the packaging.

    Product
    elegant foods Lemon Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1040-2022·2022-05-11

    Elegant Foods Macarons Recalled for Undeclared Food Coloring

    Elegant Foods is recalling macarons due to missing declarations of six synthetic food colors on the packaging. Consumers sensitive to food dyes should not consume this product.

    Product
    elegant foods Macaron Variety A, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1042-2022·2022-05-11

    Holiday Macaron Variety Recalled for Undeclared Food Colors

    Elegant Foods is recalling Holiday Macaron Variety packages due to missing label declarations for six FDA-approved food colorants. Consumers with sensitivities to dyes should not consume these products.

    Product
    elegant foods Holiday Macaron Variety, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1035-2022·2022-05-11

    Elegant Foods Fall Spice Macarons Recalled for Undeclared Food Coloring

    Elegant Foods is recalling Fall Spice Macarons because the packaging does not declare six artificial food colors: FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.

    Product
    elegant foods Fall Spice Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1036-2022·2022-05-11

    Elegant Foods Lavender Macaron Recall for Undeclared Food Colors

    Elegant Foods is recalling Lavender Macarons (code 21264A) due to undeclared food colors: FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40. Affected cases were distributed in Wisconsin.

    Product
    elegant foods Lavender Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0831-2022·2022-05-11

    Drug recall: Vancomycin HCl injection bags for manufacturing deviations

    SCA Pharmaceuticals has recalled Vancomycin HCl 1.5g injection bags due to manufacturing process deviations. The product was distributed nationwide.

    Product
    Vancomycin HCl 1.5 g in 0.9% Sodium Chloride, 500 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0924-44
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0846-2022·2022-05-11

    Lidocaine Oral Topical Solution Recalled Due to Failed Viscosity Specification

    Akorn, Inc. is recalling 66,744 bottles of Lidocaine Hydrochloride Oral Topical Solution, USP 2% (Lot #370978) nationwide because the product's viscosity was below the required specification.

    Product
    Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701, NDC 50383-775-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0837-2022·2022-05-11

    Losartan Potassium and Hydrochlorothiazide Tablets Recalled Due to AZIDO Impurity Contamination

    Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to AZIDO impurity levels exceeding acceptable manufacturing standards. The prescription blood pressure medication was distributed nationwide.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V320000·2022-05-10

    Land Rover Recalls 2022 New Range Rovers for Front Crash Sensor Defect

    Jaguar Land Rover is recalling 2022 New Range Rovers because improperly tightened fasteners may cause front crash sensors to malfunction, affecting air bag deployment.

    Product
    LAND ROVER — LAND ROVER NEW RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V319000·2022-05-10

    2022 Rivian R1T front passenger seat airbag may not deactivate for children

    Certain 2022 Rivian R1T vehicles have a malfunctioning occupant classification system that fails to deactivate the front passenger airbag when a child or child seat is present, increasing injury risk during a crash.

    Product
    RIVIAN — RIVIAN R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V318000·2022-05-10

    Braxton Creek Recalls 2022 Travel Trailers Due to LP Gas Leak Risk

    Braxton Creek RV is recalling 2022 Free Solo, Bushwhacker, and Bushwhacker Plus travel trailers because cracked LP gas fittings may cause a leak and fire.

    Product
    BRAXTON CREEK — BRAXTON CREEK BUSHWACKER, BUSHWACKER PLUS, FREE SOLO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V316000·2022-05-09

    Custom Fire Recalls Spartan Emergency Vehicles Due to Axle Defect

    Custom Fire is recalling 2021-2022 Spartan emergency vehicles because a rear axle part may fracture, potentially causing the parking brake to engage unexpectedly and increasing crash risk.

    Product
    CUSTOM FIRE — CUSTOM FIRE SPARTAN METROSTAR, SPARTAN METROSTAR RT, SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V315000·2022-05-09

    Mercedes-Benz Recalls Vehicles Due to Brake Booster Corrosion Risk

    Mercedes-Benz is recalling 2006-2012 ML, GL, and R-Class vehicles because moisture in the brake booster can cause corrosion, leading to reduced brake performance or failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ R350, ML350, AMG ML63, GL320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V313000·2022-05-09

    2023 Winnebago Ekko RV Recalled for Cracked LP Gas Fittings

    Winnebago is recalling 2021-2023 Ekko recreational vehicles because quick disconnect fittings in the LP gas system may crack, potentially causing a gas leak that could lead to fire.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V314000·2022-05-09

    Mercedes-Benz Recalls 2021 GLB 250 for Rear Axle Sensor Defect

    Mercedes-Benz is recalling 2021 GLB 250 vehicles because a rear axle sensor linkage may be improperly installed, potentially causing headlight glare that increases crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V317000·2022-05-09

    2020-2021 Tesla Model 3: Swapped Camera Terminals Impair Collision Detection

    Tesla recalls 2020-2021 Model 3 and 2021 Model Y vehicles due to incorrectly installed camera cable terminals that cause swapped camera views, impairing collision detection and automatic emergency braking.

    Product
    TESLA — TESLA MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·012-2022-EXP·2022-05-07

    Wayne Farms Recalls Undercooked Ready-to-Eat Chicken Breast Fillets

    Wayne Farms is recalling approximately 585,030 pounds of ready-to-eat chicken breast fillets that may be undercooked. The products were distributed to restaurants and retail locations in North Carolina, South Carolina, and Virginia.

    Product
    Wayne Farms LLC — Wayne Farms, LLC Recalls Ready-To-Eat Chicken Breast Fillet Products That May Be Undercooked
    Category
    Food
    Distribution
    3 states
  • CriticalUSDA FSIS·014-2022·2022-05-06

    Olympia Meats Recalls Pork Deli Meat for Undeclared Pistachios

    Olympia Meats is recalling ready-to-eat pork deli meat products because they contain undeclared pistachios, a known allergen.

    Product
    Olympia Provisions — Olympia Meats Recalls Ready-To-Eat Pork Deli Meat Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·015-2022·2022-05-06

    Pop’s Que and Stew Recalls Frozen Stew Produced Without Inspection

    Pop’s Que and Stew is recalling approximately 12,472 pounds of frozen Brunswick stew products that were produced without federal inspection. The products were distributed to retail locations in Alabama, Georgia, Mississippi, and Tennessee.

    Product
    Pop’s Que and Stew Recalls Frozen Stew Products Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·22T007000·2022-05-06

    Sumitomo and Falken Tires Recalled for Bead Separation Risk

    Sumitomo is recalling certain Sumitomo and Falken tires because a deformation near the bead could cause separation, increasing the risk of a crash.

    Product
    TIRES:BEAD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide

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