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 the agency’s own highest classification or reported deaths or serious injuries, 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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24126–24150 of 90113

  • HighNHTSA·22V575000·2022-08-04

    Jayco Recalls 2022 RVs Due to Awning Fabric Seam Separation Risk

    Jayco is recalling 2022 Greyhawk, Melbourne, Redhawk, and Entegra Odyssey RVs because a welded seam on the electric awning fabric may separate, allowing the awning to drop and increase injury risk.

    Product
    JAYCO — JAYCO, ENTEGRA GREYHAWK, ODYSSEY, REDHAWK, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V583000·2022-08-04

    2022-2023 Newmar Motorhomes Recalled for Fuel Line Fire Risk

    Newmar Corporation is recalling certain 2022-2023 motorhomes with International Thermal Research heaters due to incorrectly installed fuel lines that may leak and create a fire hazard.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, DUTCH STAR, ESSEX, NEW AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V572000·2022-08-04

    2022 Starcraft Travel Trailers: Electric Awning Seam Defect

    Starcraft is recalling certain 2022 Autumn Ridge Outfitter, Super Lite, and Super Lite Maxx travel trailers because the electric retractable awning's welded seam may separate, causing the awning to drop.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT SUPER LITE MAXX, SUPER LITE, AUTUMN RIDGE OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V576000·2022-08-04

    Ditch Witch Trailers Recalled for Incorrect Weight Rating Labels

    Charles Machine Works is recalling 2020-2022 Ditch Witch VT12, VT14, VT24, and VT14MV trailers because the vehicle certification labels list the wrong Gross Axle Weight Rating.

    Product
    DITCH WITCH — DITCH WITCH VT14, VT24, VT14MV, VT12
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V573000·2022-08-04

    Highland Ridge RV Recalls 2022 Trailers Due to Awning Fabric Defect

    Highland Ridge RV is recalling 2,448 2022 model year trailers because a welded seam on the electric retractable awning fabric may separate, allowing the awning to drop unexpectedly.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW, HIGHLAND RIDGE TT SILVERSTAR XLT, RANGE LITE AIR, OPEN RANGE ROAMER, OLYMPIA SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V581000·2022-08-04

    2022 Land Rover Range Rover Velar recall: missing audio amplifier module

    Certain 2022 Land Rover Range Rover Velar vehicles were manufactured without an Audio Amplifier Module, causing loss of critical safety features including seat belt reminders and ADAS warnings. Owners should contact Land Rover at 1-800-637-6837 for free repair.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER VELAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V582000·2022-08-04

    Kenworth T680 Tractor Trailers Recalled for Fuel Tank Wear Risk

    PACCAR is recalling approximately 630 2022-2023 Kenworth T680 tractor trailers. The mud flap may contact the fuel tank during operation, causing wear that could result in fuel spillage and increase crash or injury risk.

    Product
    KENWORTH — KENWORTH T680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V584000·2022-08-04

    Newmar Motorhomes: Improperly Connected LPG Service Valves Risk Propane Leaks

    Newmar is recalling certain 2022 and 2021-2023 motorhomes due to improperly connected LPG service valves that may leak propane. A leak in the presence of an ignition source can increase fire risk.

    Product
    NEWMAR — NEWMAR BAY STAR SPORT, CANYON STAR, KOUNTRY STAR, BAY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V571000·2022-08-04

    Jayco Recalls 2022-2024 Travel Trailers Due to Awning Seam Defect

    Jayco is recalling specific 2022-2024 travel trailers and fifth wheels because a welded seam on the electric retractable awning may separate, causing the awning to drop.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER, JAYCO FIFTH WHEEL JAY FLIGHT SLX, SEISMIC, EAGLE HT, PINNACLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22197·2022-08-04

    Makita Cordless Hedge Trimmers Recalled for Missing Blade Guard

    Makita U.S.A. Inc. is recalling about 2,600 cordless hedge trimmers because the teal-colored guard on the shear blade may be missing, posing a laceration hazard to users.

    Product
    Cordless hedge trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1292-2022·2022-08-03

    Insulin Glargine Prefilled Pens Recalled for Missing Label

    Mylan Pharmaceuticals is recalling Insulin Glargine prefilled pens (lot BF21002895) distributed nationwide because some pens lack labels, which could prevent patients from properly identifying and administering the medication.

    Product
    Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL (U-100), 3 mL prefilled pens (NDC 49502-394-71), packaged in cartons of 5 prefilled pens (NDC 49502-394-75), Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 15317, Manufactured for: Mylan…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1395-2022·2022-08-03

    CereLink ICP Monitor recalled for out-of-range pressure readings

    Integra LifeSciences is recalling CereLink ICP Monitors due to electrical interference causing intracranial pressure readings to drift out of range. Affected devices may display an error message indicating sensor or extension cable failure.

    Product
    CereLink ICP Monitor; Catalog No. 826820, 826820P. Intracranial pressure monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1397-2022·2022-08-03

    BD Intraosseous Needle Kits recalled for mechanical failure and safety defects

    BD Intraosseous Needle Kits have been recalled due to mechanical failures that could prevent emergency vascular access. Affected units nationwide and in Canada may experience stylet removal problems, safety mechanism failures, or driver malfunction.

    Product
    Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/ BD Manual Driver Needle Kit 15mm x 15Ga, D015251NK/ BD Needle Kit for Powered Driver 25mm x 15Ga, D015251MK/ BD Manual Driver Needle Kit 25mm x 15Ga…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1507-2022·2022-08-03

    Za'atar Seasoning recalled for potential Salmonella in oregano

    Fuchs North America is recalling Za'atar Seasoning (lot 252491) because an oregano sub-ingredient tested positive for Salmonella. The product was distributed to one commercial buyer.

    Product
    Za'atar Seasoning, Cust Part # Lot No. 252491, NET WT 50 lbs bag in a box. One bag per box, GT 74862, Lot code: 252491.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1286-2022·2022-08-03

    Nifedipine WSP Ointment Recalled Due to Potency Variability

    Valor Compounding Pharmacy is recalling Nifedipine WSP 0.2% Ointment due to potency variability. Some batches may be subpotent or superpotent, affecting safety and efficacy.

    Product
    Nifedipine WSP 0.2% Ointment, 60 gram tubes, Rx only, Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1376-2022·2022-08-03

    ABACUS TPN Calculation Software recalled for medication error risk

    Baxter Healthcare's ABACUS TPN calculation software poses a potential risk of medication error. The FDA issued a Class I recall; healthcare providers should contact the manufacturer for guidance.

    Product
    ABACUS TPN (Total Parenteral Nutrition) Calculation software, Product codes: 8300-0167 (Abacus V3.1 CE), 8300-0168 (Abacus V3.1 SE), 8300-0169 (Abacus V3.1 ME), 8300-0191 (Abacus V3.2 CE), 8300-0192 (Abacus V3.2 SE), 8300-0193 (Abacus V3.2 ME), 8300-3391 (Abacus V3.3 CE)…
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·22V566000·2022-08-03

    Kalmar Recalls 2021-2022 Ottawa T2 Tractors Due to Steering Gear Defect

    Kalmar is recalling 2021-2022 Ottawa T2 terminal tractors because incorrectly assembled steering gears may fracture, causing loss of steering control and increasing crash risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V567000·2022-08-03

    Audi Recalls One 2022 SQ5 Sportback for Rear Lid Connection Issue

    Volkswagen Group of America is recalling one 2022 Audi SQ5 Sportback because the rear lid connections may be improper, potentially reducing crash protection.

    Product
    AUDI — AUDI SQ5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1293-2022·2022-08-03

    Irbesartan Blood Pressure Tablets Recalled Due to Failed Dissolution

    Jubilant Cadista is recalling 9,600 bottles of Irbesartan Tablets (150mg) nationwide due to failed dissolution specifications. Affected lot IB220023A expires 08/2022.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1512-2022·2022-08-03

    Dole Spring Mix Recalled for Potential Hairy Nightshade Contamination

    Dole Fresh Vegetables is recalling Simply Nature Organic Spring Mix and Marketside Spring Mix due to potential contamination with hairy nightshade. The recalled products were distributed to Ohio, Illinois, Indiana, and Tennessee.

    Product
    Simply Nature Organic Spring Mix 16 oz. Marketside Spring Mix 11 oz. and 5 oz.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1480-2022·2022-08-03

    Medtronic Cobalt Implantable Cardioverter Defibrillators Recalled for Cathode Component Defect

    Medtronic is recalling three Cobalt Implantable Cardioverter Defibrillators (CRT-D) due to a manufacturing error that may have resulted in a cathode component being out of specification. Affected patients should contact their physician.

    Product
    Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1455-2022·2022-08-03

    Abbott Alinity c Hemoglobin Reagent Kit may produce falsely elevated test results

    Abbott Laboratories is recalling the Alinity c Hemoglobin Reagent Kit because the ARCHITECT and Alinity c assays can generate falsely elevated Hemoglobin A1c results.

    Product
    REF: 08P4320, Alinity c Hemoglobin Reagent Kit, IVD, CE, R1 5 x 46.0 mL, R2 5 x 18.3 mL, A1cDL 5 x 67.6 mL
    Category
    Medical Device
    Distribution
    43 states