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.

7776–7800 of 29121

  • SevereFDA (Food)·F-0988-2021·2021-09-29

    Joy Coriander Chutney Recalled for Undeclared Sulfites

    Joy Coriander Chutney (8 oz, best by 07/30/22) is being recalled because it contains high levels of undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.

    Product
    2. "***JOY***Coriander Chutney***NET WT 8 OZ (228g)***07 28 BEST BY 073022***INGREDIENTS: CORIANDER, GREEN CHILLIES, COCONUT, SUGAR, SALT, SPICES, VINEGAR, STABILIZERS (GUAR, TRAGAGANTH AND XANTHAN), CITIRC ACID, SODIUM BENZOATE AS PRESERVATIVE & ARTIFICIAL COLORS (FD&C BLUE 1 &
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0827-2021·2021-09-29

    Arformoterol Tartrate Inhalation Solution Recall Due to Sterility Assurance

    Glenmark Pharmaceuticals is recalling Arformoterol Tartrate Inhalation Solution 15 mcg/2 mL nationwide because the manufacturer lacks assurance of sterility for affected lots.

    Product
    Arformoterol Tartrate Inhalation Solution 15 mcg*/2 mL For Oral Inhalation Only Rx Only Manufactured by: Glenmark Pharmaceuticals Inc., USA Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430 a) 60x2 mL Sterile Unit-Dose Vials NDC 68462-833-65;
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1009-2021·2021-09-29

    Banquet Cut European Style Cold Smoked Salmon Recalled for Botulinum Risk

    Seabear Company is recalling Banquet Cut European Style Cold Smoked Salmon due to potential for growth of Clostridium botulinum. The affected product was distributed in Arizona, California, and Georgia.

    Product
    Banquet Cut European Style Cold Smoked Salmon, Item Number 2-92845, brand Gerard and Dominique Seafoods, packaged in pouch, net wt. per pouch is random, frozen, UPC of pouch: 2 92845 00250 3. The storage/thawing instructions on the pouch is read in parts: "***KEEP FROZEN UNTIL
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1006-2021·2021-09-29

    Golden Natural Product Dried Apricots Recalled for Undeclared Sulfites

    Golden Natural Product Inc. brand Dried Apricot Subkhon products (with bone and jumbo varieties) are being recalled because they contain high levels of undeclared sulfites. The affected products have lot number GC005 and expiration date 2023.

    Product
    Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and Golden Natural Product Inc. brand Dried Apricot Subkhon Jumbo, Net Wt. 16 oz (1 lb) 454 g Manufactured and Packed by: Gardencells LLC, Urgut, Samarkand region Republic of Uzbekist
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2469-2021·2021-09-29

    Multiple Ultrasound Gel Products Recalled for Potential Bacterial Contamination

    Ultrasound gels sold under multiple brand names have been recalled due to potential bacterial contamination. Approximately 100,114 units distributed nationwide between August 2018 and August 2021 are affected.

    Product
    Ultrasound Gel labeled under the following brand names: MediChoice Ultrasound Gel, Athena Liquasonic Ultrasound Gel, Eco-Med EcoGel Ultrasound Gel, MAC Medical Supply Ultrasound Gel, Eco-Med EcoGel 200 Blue High Velocity Ultrasound Gel, Eco-Med EcoGel 200 Multi-Purpose Ultrasoun
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0830-2021·2021-09-29

    Avicel RC-591 NF Bulk Powder Recalled for Microbial Contamination

    DuPont Nutrition USA is recalling Avicel RC-591 NF bulk powder (lot #2173766940) due to out-of-specification microbial contamination. The product was distributed as a component in finished drug formulations nationwide.

    Product
    Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF, bulk powder, 80.0 KG drum, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V753000·2021-09-28

    Tiffin Wayfarer RV Water Tank Mounting Defect Increases Crash Risk

    Tiffin Motorhomes is recalling 2018-2022 Wayfarer RVs because the rear water tank mounting bolts can fail, causing the tank to fall onto the exhaust pipe. This affects vehicle stability and increases crash risk.

    Product
    TIFFIN — TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V617000·2021-09-27

    Toyota Recalls 2019-2020 Yaris Models for Fuel Pump Defect

    Toyota is recalling 2019-2020 Yaris vehicles because a fuel pump impeller may crack, potentially causing engine stalls and increasing crash risk.

    Product
    TOYOTA — TOYOTA YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V752000·2021-09-27

    Spartan K3 and K4 Recalled for Power Steering Pump Defect

    Shyft Group is recalling 2020-2022 Spartan K3 and K4 RVs because a machining defect may cause the power steering pump shaft seal to break, resulting in a loss of power steering assist.

    Product
    SPARTAN — SPARTAN K4, K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·034-2021·2021-09-26

    Nestle Recalls DiGiorno Pepperoni Pizza Due to Undeclared Soy Allergen

    Nestle is recalling approximately 27,872 pounds of frozen DiGiorno Crispy Pan Crust Pepperoni Pizza because some cartons contain undeclared soy protein.

    Product
    Nestlé USA Inc. Recalls Frozen DiGiorno Crispy Pan Crust Pepperoni Pizza Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·033-2021·2021-09-25

    Ajinomoto Recalls Raw Frozen Chicken Potstickers Due to Plastic Contamination

    Ajinomoto Foods North America is recalling raw, frozen chicken and vegetable potstickers that may contain clear flexible and hard plastic.

    Product
    Ajinomoto Foods North America Inc Recalls Raw, Frozen Chicken and Vegetable Potsticker Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V748000·2021-09-24

    MCI Motorcoaches Recalled for Main Distribution Panel Fire Risk

    Motor Coach Industries is recalling specific 2017-2021 motorcoaches because a circuit board in the battery compartment may fail, potentially causing a fire or unexpected shutdown.

    Product
    MCI — MCI D45 CRT LE, D4000ISTV, D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V736000·2021-09-23

    Altec Recalls 2011-2016 Aerial Devices Due to Mounting Frame Cracks

    Altec is recalling 2011-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V742000·2021-09-23

    2022 Nissan Pathfinder: Third-Row Headrests May Detach or Move

    Nissan is recalling 2022 Pathfinder vehicles because the third-row headrests may move or detach due to improper welds or misaligned components. Detached headrests could fail to restrain occupants in a crash, increasing injury risk.

    Product
    NISSAN — NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V733000·2021-09-23

    DRV Recalls 2018-2021 Elite and Mobile Suites Due to Brake Caliper Defect

    DRV Suites is recalling 2018-2021 Elite and Mobile Suites because brake caliper clips may bend, causing the caliper to unseat and increasing crash risk.

    Product
    DRV — DRV MOBILE SUITES, MOBILE SUITE, ELITE SUITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V732000·2021-09-23

    Volkswagen Recalls 2018 Tiguan Vehicles Due to Roof Reinforcement Defect

    Volkswagen is recalling 2018 Tiguan vehicles because an incorrect roof reinforcement assembly may have been installed during prior repairs, potentially compromising structural integrity and airbag deployment.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V740000·2021-09-23

    Braun Recalls Demers Ambulances Due to Fire Risk from Damaged Wires

    Braun Ambulances is recalling 2020-2021 Demers MXP153 vehicles because damaged electrical wires and oxygen tubes may increase fire risk.

    Product
    DEMERS AMBULANCES — DEMERS AMBULANCES MXP153 FORD F-SERIES, MXP153 DODGE RAM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0975-2021·2021-09-22

    Purim Health Products EpiGenius Kids Creamy Chocolate Recalled for Undeclared Milk

    Purim Health Products EpiGenius Kids Creamy Chocolate powder is recalled due to undeclared milk in an MCT powder ingredient. The product was not labeled to indicate the presence of milk, which is a common allergen.

    Product
    Purim Health Products: EpiGenius Kids Creamy Chocolate; 630 Grams, individually packed pouches. Daily Superfoods. This high protein, whole-food blend is an excellent source of vitamins A, C, D and E and contains superfruits and superveggies, along with healthy fat, fiber and
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0796-2021·2021-09-22

    Florance Morris ANTISEPTIC Hand Sanitizer Recalled for Methanol Contamination

    Florance Morris ANTISEPTIC Hand Sanitizer (70% ethyl alcohol) in 8.45 fl oz and 33.81 fl oz bottles is being recalled due to methanol contamination found in some lots. All lots are affected due to manufacturing under the same conditions as contaminated products.

    Product
    Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V746000·2021-09-22

    Ford Recalls 2011-2013 Explorers for Rear Suspension Defect

    Ford is recalling 2011-2013 Explorers in 23 states and D.C. because a rear suspension part may fracture, causing loss of steering control.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0965-2021·2021-09-22

    Full Tilt Dark Chocolate Ice Cream Recall for Inadequate Pasteurization

    Full Tilt Ice Cream, LLC is recalling Dark Chocolate ice cream in 16oz pints and 3-gallon tubs because the ice cream mix did not meet pasteurization specifications. The product was distributed in Washington.

    Product
    Dark Chocolate, Full Tilt Ice Cream brand, packaged in 16oz pre packed pints and 3 gallon tubs. UPC on pint container only: 00856962005276.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0804-2021·2021-09-22

    Spironolactone Ophthalmic Solution Recalled for Lack of Sterility Assurance

    Greenpark Compounding Pharmacy is recalling Spironolactone Ophthalmic Solution 0.005 mg/mL due to lack of assurance of sterility. The 15 mL bottles were distributed nationwide.

    Product
    Spironolactone Ophthalmic Solution 0.005 mg/mL, 15 mL bottles, Rx only, Greenpark Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2428-2021·2021-09-22

    Angiographic Catheter Recall: Cordis SUPER TORQUE Entrapment and Dislodgement Risk

    Cordis is recalling its SUPER TORQUE MB Angiographic Catheter worldwide because it may become entrapped between endovascular devices and the vessel wall. This entrapment can cause marker band movement or dislodgement.

    Product
    Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0800-2021·2021-09-22

    Lidocaine Hydrochloride Topical Solution Recalled for Superpotency

    Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution, USP 4% due to the product being superpotent. The recall affects 32,544 bottles distributed nationwide in the United States and Canada.

    Product
    Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New Jersey 08310, NDC 52565-009-50.
    Category
    Drug
    Distribution
    Distributed nationwide