The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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23426–23450 of 26079

  • HighFDA (Devices)·Z-0379-2022·2021-12-22

    Olympus EVIS EXERA II Duodenovideoscope Recalled for Contamination Risk

    Olympus TJF-Q180V duodenovideoscopes with adhesive deterioration or damage may pose infection risk due to endoscope contamination. Approximately 14,447 units are affected.

    Product
    EVIS EXERA II DUODENOVIDEOSCOPE OLYMPUS TJF-Q180V Model Number: TJF-Q180V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0365-2022·2021-12-22

    Orthopedic Femur Plate Recalled for Incorrect MRI Safety Information

    Smith & Nephew is recalling 35 units of EVOS Condylar Medial Distal Femur Plate due to incorrect MRI scanning safety information in the product instructions. The instructions contained erroneous data that could affect patient safety during MRI procedures.

    Product
    smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, L, 5H, 115MM, REF 72573102
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0375-2022·2021-12-22

    Cardinal Health Recalls RoyalSilk Surgical Gowns for Compromised Packaging Seals

    Cardinal Health is recalling 364,481 units of RoyalSilk Non-Reinforced Surgical Gowns due to potential for open packaging seals that could compromise sterility. The recalled units were distributed worldwide.

    Product
    RoyalSilk Non-Reinforced Surgical Gowns Large SKU: 9518
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0330-2022·2021-12-22

    Kool-Aid Tropical Punch Drink Mix Recalled for Glass and Metal Contamination

    Kraft Heinz Foods is recalling Kool-Aid Tropical Punch "on the go" 10-pack drink mix powder due to potential contamination with glass and metal fragments. The affected product was distributed nationwide and internationally.

    Product
    Kool-Aid Tropical Punch "on the go" 10 pack net wt. 6.6 oz. drink mix powder UPC 043000023464
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0374-2022·2021-12-22

    Cardinal Health Surgical Gowns Recalled Due to Compromised Packaging Seals

    Cardinal Health Poly-Reinforced Surgical Gowns (XX-large, SKU 9070) are recalled due to potential open packaging seals that could compromise sterility. Approximately 29,893 units distributed worldwide may be affected.

    Product
    Cardinal Health Poly-Reinforced Surgical Gowns XX-large SKU: 9070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0376-2022·2021-12-22

    RoyalSilk Surgical Gowns Recalled for Potential Sterility Compromise

    Cardinal Health is recalling 270,839 units of RoyalSilk Non-Reinforced Surgical Gowns (X-large, SKU 9548) due to potential packaging seal failures that could compromise sterility.

    Product
    RoyalSilk Non-Reinforced Surgical Gowns X-large SKU: 9548
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0285-2022·2021-12-22

    Yeast Extract Ajirex Recalled for Potential Salmonella Contamination

    Mitsubishi International Food Ingredients is recalling Yeast Extract Ajirex in 15 kg bags due to potential Salmonella contamination. The product was distributed to Georgia, Illinois, Pennsylvania, and Texas.

    Product
    Yeast Extract Ajirex in 15 kg PE bag in carton box
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0284-2022·2021-12-22

    Ripple Dairy-Free Plant-Based Milk Recalled for Bacillus Cereus

    Ripple Foods is recalling 48 fl oz bottles of Ripple Dairy-Free Plant-Based Milk due to the detection of Bacillus Cereus in one lot. The contamination was identified during an FDA investigation.

    Product
    Ripple Dairy-Free. As It Should Be 8g Plant Based Protein; Half the Sugar of Dairy Milk PET bottle with twist cap 50% More Calcium that Dairy Milk. Keep refrigerated. Fresh for 7-10 days after opening. 48 fl oz. (1.5 qt) ((1.42L) - 6 x 48 ox. bottles per case Ingredients: Wate
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0385-2022·2021-12-22

    Activ5 Smart Fitness Device Recalled for Inaccurate Force Measurement

    Activbody is recalling the Activ5 smart fitness device due to manufacturing defects causing inaccurate force measurements, which may lead to incorrect treatment planning. The device was distributed nationwide.

    Product
    Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5, the first isometrics-based smart strength training and rehabilitation device.
    Category
    Medical Device
    Distribution
    43 states
  • HighFDA (Devices)·Z-0369-2022·2021-12-22

    Cardinal Health Surgical Gowns Recalled for Potential Packaging Seal Defects

    Cardinal Health is recalling 169,262 SmartSleeve surgical gowns due to potential package seal defects that could compromise sterility. Multiple affected lot numbers span 2020-2021 production with worldwide distribution.

    Product
    SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns-Large SKU: 9011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0387-2022·2021-12-22

    Cook Flexor Check-Flo Introducer recalled for size mislabeling

    Cook Inc. is recalling the Flexor Check-Flo Introducer due to mislabeled packaging where 6FR devices may be labeled as 7FR or vice versa. This size mislabeling could result in selection of the wrong device size.

    Product
    Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-6.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44154 Intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Food)·F-0324-2022·2021-12-22

    Country Time "On The Go" Lemonade Drink Mix Powder Recall

    Kraft Heinz Foods Company is recalling Country Time "On The Go" Lemonade 10-pack drink mix powder due to potential glass and metal contamination in the product.

    Product
    Country Time "on the go" Lemonade 10 pack net wt. 6.7 oz. drink mix powder UPC 043000010983
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0328-2022·2021-12-22

    Kool-Aid Ice Blue Raspberry Lemonade Drink Mix Recalled for Glass and Metal

    Kraft Heinz Foods Company is recalling Kool-Aid ice blue raspberry lemonade drink mix powder (20 oz.) due to potential glass and metal contamination in the product.

    Product
    Kool-Aid ice blue raspberry lemonade drink mix powder 20 oz. UPC 043000954072
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0361-2022·2021-12-22

    Medline Venous Access Pack-LF Recalled for Expired Saline Component

    Medline is recalling Venous Access Pack-LF Convenience Kits because the included saline solution component expired before the kit's labeled expiration date, creating a quality and safety issue.

    Product
    Venous Access Pack-LF Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00B000·2021-12-21

    Tesla Model S Hood Latch Misalignment Could Cause Unexpected Hood Opening During Driving

    Tesla is recalling 2014-2021 Model S vehicles due to a misaligned front trunk latch assembly that may prevent the secondary hood latch from engaging. This could allow the hood to open unexpectedly during driving, obstructing the driver's view and increasing crash risk.

    Product
    TESLA — 2018 TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00A000·2021-12-21

    2022 Jeep Wagoneer and Grand Wagoneer Rearview Display Software Defect

    Certain 2022 Jeep Wagoneer and Grand Wagoneer vehicles have a radio software defect that may prevent the rearview camera display from functioning, reducing rear visibility and increasing crash risk. Dealers will reprogram the radio software free of charge.

    Product
    JEEP — 2022 JEEP WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V997000·2021-12-20

    2022 Entegra Vision Motorhomes Recalled for Melting Wiring Harness

    Jayco is recalling certain 2022 Entegra Vision motorhomes because the main chassis wiring harness may be positioned too close to the exhaust manifold, causing the wiring to melt. This can lead to vehicle stall and increased crash risk.

    Product
    ENTEGRA — 2022 ENTEGRA VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V990000·2021-12-17

    2020 Mercedes-Benz A220 suspension recall due to corroding axle carrier

    Mercedes-Benz is recalling certain 2019-2020 A220 and other model vehicles because the front axle carrier may corrode and fail, potentially causing loss of steering control. Dealers will inspect and replace the carrier for free.

    Product
    MERCEDES-BENZ — 2020 MERCEDES-BENZ A220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V988000·2021-12-17

    Forest River Cardinal fifth wheel vehicles recalled for carbon monoxide risk

    Forest River is recalling 2020-2022 Cardinal fifth wheels because the generator compartment may not be properly sealed, potentially allowing carbon monoxide into the vehicle. Owners should contact dealers for free inspection and repair.

    Product
    FOREST RIVER — 2022 FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V979000·2021-12-16

    2021-2022 Ford Mustang Mach-E and 2022 Maverick seat belt attachment recall

    Ford is recalling 2021-2022 Mustang Mach-E and 2022 Maverick vehicles due to improperly attached rear seat belt buckles. The defect may prevent proper occupant restraint in a crash, creating an injury risk.

    Product
    FORD — 2021 FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22712·2021-12-16

    Northern Lights Alaura Two-Tone Jar Candles Recall Due to Laceration and Fire Hazards

    Northern Lights is recalling Alaura Two-Tone Jar Candles sold at Costco because the glass containers can shatter, crack, or break while burning, posing laceration and fire hazards. The company has received 138 reports of breakage, including three reports of laceration injuries.

    Product
    Alaura Two-Tone Jar Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V987000·2021-12-16

    2021 Honda Rebel 1100 Radiator Cap May Leak Hot Coolant

    Honda is recalling 2021 Rebel 1100 motorcycles because the radiator cap may have been improperly formed, creating an insufficient seal. A leaking cap could spray hot coolant, increasing risk of injury or crash.

    Product
    HONDA — 2021 HONDA REBEL 1100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V980000·2021-12-16

    2021 Ford Mustang side curtain air bags may not inflate properly

    Ford is recalling 2021 Mustang vehicles because the side curtain air bag inflators may have been manufactured with incorrect gas pressure, potentially resulting in improper inflation during a crash.

    Product
    FORD — 2021 FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22713·2021-12-16

    Karmas Far Infant Bath Seats Recalled for Drowning Hazard

    Karmas Far infant bath seats fail federal safety standards and can tip over during use, posing a drowning hazard to babies. About 900 units sold online between August 2017 and October 2021 are affected. No injuries have been reported.

    Product
    Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide