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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21076–21100 of 27451

  • HighFDA (Devices)·Z-1823-2022·2022-10-05

    CooperSurgical incubator humidifier kit recall due to sterile barrier breach

    CooperSurgical is recalling 5,182 humidifier bottle and filter kits for BT37 Mark II incubators due to potential sterile barrier damage from packaging defects. This could result in use of unsterilized components, risking embryo contamination.

    Product
    Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark II Benchtop Incubator (AY200246)
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-1777-2022·2022-10-05

    Collagen Dental Wound Dressing Recalled Due to Potential Sterility Compromise

    Collagen Matrix Inc is recalling Collagen Dental Wound Dressing products because packaging may not be sealed, potentially compromising sterility. Affected products were distributed to medical distributors in six states.

    Product
    Collagen Dental Wound Dressing - Bovine Dermis Tap, 25mm x 75mm Product was distributed under the following brand names: 1) Cytoplast RTMTAPE, 25mm x 75mm 2) GIBSON Healthcare, 25mm x 75mm 3) MaxxTape, 2.5cm x 7.5cm x 0.1cm 4) NEOTAPE, 25mm x 75mm 5) Karl Schuma
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Drugs)·D-1543-2022·2022-10-05

    FDA Recalls Neoral Cyclosporine for Out-of-Specification Ethanol Content

    Novartis is recalling Neoral cyclosporine 25 mg capsules nationwide due to a manufacturing quality deviation. Lot APCD162 (expiration 01/2023) was found to have out-of-specification ethanol content during stability testing.

    Product
    NEORAL — NEORAL (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1824-2022·2022-10-05

    Cook guidewires recalled for compromised sterility due to packaging breach

    Cook Incorporated is recalling Amplatz extra Stiff Wire Guides because packaging seals may be completely breached, potentially compromising device sterility.

    Product
    Amplatz extra Stiff Wire Guide, Stiff Guidewire (OUS ONLY); Reference Part Number: THSF-35-145-AES-SGH (GPN G06801) THSF-38-80-AES-SGH (GPN G06874)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1789-2022·2022-10-05

    Alida's Wheat Saoka Pita Bread recalled for undeclared soy allergen

    Alida's Wheat Saoka Pita Bread is recalled for undeclared soy lecithin found in the pan-grease canola oil. The product label does not disclose soy, posing a risk to soy-allergic consumers. Distributed in Washington state only.

    Product
    Alida's Wheat Saoka Pita Bread, 5 pieces per package. Net Wt. 16.25 oz. UPC 8 60004 65931 0. Product contains ingredients: Wheat Flour, White Flour, Water, Wheat Gluten, Yeast, Sorbitan monostearate, ascorbic acid, salt, Canola Oil. CONTAINS: Wheat, Gluten.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1786-2022·2022-10-05

    Mobile X-Ray System Recalled for Software Calibration Error in Radiation Dose Meter

    Micro-X Rover mobile X-ray systems recalled due to a software calibration error that causes incorrect radiation dose readings. The malfunction may impede proper radiation exposure management decisions.

    Product
    MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1847-2022·2022-10-05

    Medical Guidewire Recalled for Packaging Defect Affecting Sterility

    Cook Incorporated is recalling Movable Core Wire Guide (Tefcor) guidewires due to a packaging defect where the chevron seal may be breached, potentially compromising device sterility.

    Product
    Movable Core Wire Guide (Tefcor), Guidewire (OUS ONLY) Reference Part Number/GPN TMT-35-145 G01677
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1834-2022·2022-10-05

    Cook Guidewire Devices Recalled for Packaging Defect and Sterility Compromise

    Cook Incorporated is recalling fixed core wire guide devices due to packaging defects that may compromise device sterility. Approximately 5,669 units were distributed in the US and 5,286 internationally.

    Product
    Fixed Core Wire Guide (Straight), Guidewire Reference Part Number/GPN: C-SF-18-30 G02261 C-SF-25-40 G01937 TSF-18-260 G00590 C-SF-25-50 G01938 TSF-35-180 G00652 C-SF-18-40 G02255 TSF-25-145 G00617 TSF-32-145 G00638 C-SF-15-50 G02274 TSF-18-145 G00587 TSF-18-50 G00593
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1843-2022·2022-10-05

    Torq-Flex Wire Guide Guidewires Recalled Due to Packaging Seal Defect

    Cook Incorporated is recalling Torq-Flex Wire Guide guidewires because the packaging chevron seal may be breached, potentially compromising device sterility. The affected units were distributed domestically and internationally.

    Product
    Torq-Flex Wire Guide Australian Modification, Guidewire Reference Part Number/GPN STF-18-40-AUST G07304
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1842-2022·2022-10-05

    Cook Rosen Curved Wire Guide Recall: Sterility Concerns

    Cook Incorporated is recalling specific lots of Rosen Curved Wire Guide guidewires due to a complete breach of the packaging seal that may compromise device sterility. Affected devices were distributed nationwide in the US and worldwide.

    Product
    Rosen Curved Wire Guide, Guidewire Reference Part Number/GPN THSCF-35-220-1.5-ROSEN G01623 THSCF-35-80-1.5-ROSEN G01774 THSCF-35-180-1.5-ROSEN G01264 THSCF-35-145-1.5-ROSEN G01261
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0742-2022·2022-10-05

    VIDAS CMV IgM diagnostic test kits recalled for invalid calibrations

    bioMerieux is recalling 480 VIDAS CMV IgM test kits with invalid calibrations distributed across 18 U.S. states. The calibration errors may affect diagnostic test accuracy.

    Product
    VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Devices)·Z-1815-2022·2022-10-05

    Olympus POWERSEAL 5MM Electrosurgical Sealer Recalled Due to Loose Retention Ring

    Olympus is recalling POWERSEAL 5MM electrosurgical sealers due to a component defect that may cause the rotation knob to loosen and delay surgical treatment.

    Product
    Olympus POWERSEAL 5MM, 44CM, CURVED JAW SEALER & DIVIDER, DOUBLE-ACTION Model Number: PS-0544CJDA. An electrosurgical device use in laparoscopic/minimally invasive or open surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V737000·2022-10-04

    2022-2023 Coachmen Recreational Vehicles Recall: Unintended Awning Movement

    Forest River is recalling certain 2022-2023 Coachmen recreational vehicles with a software issue that may cause the awning to unintentionally extend or retract while parked, increasing injury risk. Owners should contact dealers for a free ECM software update.

    Product
    COACHMEN — 2022 COACHMEN BEYOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V728000·2022-09-30

    Crossroads and Dutchmen Trailers Recalled for Loose Axle U-Bolts

    Keystone RV is recalling 2021-2022 Crossroads Redwood, Dutchmen Voltage, and Yukon trailers for improperly tightened axle U-bolts that may cause loss of vehicle control and crash risk.

    Product
    CROSSROADS — 2021 CROSSROADS REDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V731000·2022-09-30

    Ford F-53 Rear Stabilizer Brackets May Separate from Vehicle

    Ford is recalling 2020-2021 F-53 recreational vehicles because rear stabilizer bar attachment brackets may break and separate, creating a road hazard and increasing crash risk. Dealers will inspect and replace the brackets free of charge.

    Product
    FORD — 2020 FORD F53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V730000·2022-09-30

    2022 Ford Maverick brake lights may illuminate unintended due to ABS defect

    Ford is recalling 2022 Maverick vehicles with an ABS module defect that may cause brake lights to illuminate without driver input. This could confuse other drivers and increase crash risk.

    Product
    FORD — 2022 FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V729000·2022-09-30

    2021-2022 Forest River Travel Trailers: Fresh Water Tank Dislodgement

    Forest River is recalling 2021-2022 Ozark, Wildwood, and Salem travel trailers because the fresh water tank may dislodge when full or overfilled, creating a road hazard and increasing crash risk.

    Product
    FOREST RIVER — 2021 FOREST RIVER OZARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V733000·2022-09-30

    2020 Mercedes-Benz CLS450 improperly secured battery defect recall

    Mercedes-Benz is recalling 2019-2022 CLS450 and related models. The 12V battery in the trunk may not be properly secured, which could cause electrical failure and disable safety features like the emergency call system, hazard lights, and automatic door locks in a crash.

    Product
    MERCEDES-BENZ — 2020 MERCEDES-BENZ CLS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22235·2022-09-29

    Custom Elevator Residential Elevators Recalled for Child Entrapment Hazard

    Custom Elevator is recalling residential elevators due to a hazardous gap between the exterior landing door and interior car door that can trap young children. One child died from entrapment in July 2021.

    Product
    Residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22234·2022-09-29

    Cambridge Elevating Residential Elevators Recalled for Child Entrapment Hazard

    Cambridge Elevating residential elevators may have a hazardous gap between exterior and interior doors that can trap young children, posing a risk of serious injury or death when the elevator moves. About 1,700 units sold nationwide from 1991 through August 2022 are affected.

    Product
    Residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22779·2022-09-29

    E-Z-GO RXV Personal Transportation Vehicles Steering System Failure Recall

    Textron Specialized Vehicles recalled about 34,000 E-Z-GO RXV personal transportation vehicles (golf carts) because steering knuckles and A-arms can break during impact, causing loss of steering control and crash hazards.

    Product
    E-Z-GO RXV Personal Transportation Vehicles (PTV)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V727000·2022-09-29

    2022 Lucid Air: Tow Eye Bracket Detachment Risk During Towing

    Lucid is recalling certain 2022 Air vehicles where the front tow eye bracket may be inadequately attached to the subframe and can detach during towing. This could separate the vehicle from the tow truck, increasing crash risk.

    Product
    LUCID — 2022 LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22232·2022-09-29

    North States Industries Recalls Toddleroo Rotating Cabinet Latches for Choking Risk

    North States Industries is recalling about 103,000 Toddleroo Rotating Cabinet Latches because the latching button can detach, posing a choking hazard to young children. The company has received 19 reports of the button dislodging, including one report of a child gagging.

    Product
    Toddleroo Rotating Cabinet Latches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22237·2022-09-29

    HyperJuice 130W USB-C Battery Packs Recalled for Fire Hazard

    Hyper Products is recalling HyperJuice 130W USB-C Battery Packs because they can overheat while charging and pose a fire hazard. Two reports of overheating have resulted in smoke, melting, and property damage.

    Product
    HyperJuice 130W USB-C Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide