The Recall Desk

State

Wyoming product recalls

73,584 recalls have nationwide distribution and so reach Wyoming. 3,226 additional recalls listed Wyoming specifically in their distribution scope.

What the numbers show

Total
3,226
Critical
759
Severe
684
Most recent
2026-09-23

Of the 3,226 recalls naming Wyoming we have scored against our rubric, 759 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 684 (21%) are Severe.

Which agencies issued them

These figures cover only the 3,226 recalls whose distribution notice names Wyoming specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24051–24075 of 76810

  • ModerateFDA (Drugs)·D-0863-2021·2021-10-06

    Althaea Officinalis 4X Homeopathic Medicine Recalled for Failed Identification Testing

    Washington Homeopathic Products is recalling Althaea Officinalis 4X, Iritable Bladder homeopathic medicine (Lot # 29377, Exp 8/17/2026) distributed nationwide because testing results failed to meet specifications for product identification.

    Product
    Althaea Officinalis 4X, Iritable Bladder* packaged as Sucrose/Lactose Pills, 4 Dram, WHP Homeopathic Medicine, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0877-2021·2021-10-06

    Washington Homeopathic Products Quebracho 4C Fever Medicine Recall

    Washington Homeopathic Products is recalling Quebracho 4C Fever homeopathic medicine (Lot #28930, expiration 8/17/2026) distributed nationwide due to out-of-specification test results from identification testing.

    Product
    Quebracho 4C, Fever*, 20% Alcohol, Packaged as 100ml, WHP Homeopathic Medicine, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·21V776000·2021-10-05

    Spartan RV Chassis K1 and K2 Recalled for Loose Rear Suspension Fasteners

    Shyft Group is recalling certain 2020-2022 Spartan K1 and K2 RV chassis because rear suspension fasteners may not have been tightened properly, which could allow the rear axle to shift and increase crash risk. Free repair is available.

    Product
    SPARTAN — SPARTAN K1, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V774000·2021-10-04

    Nissan Recalls Hybrid SUVs for Software-Related Loss of Drive Power

    Nissan is recalling certain 2014-2017 hybrid SUVs because software may shut down the engine, causing a loss of drive power and increasing crash risk.

    Product
    INFINITI — INFINITI, NISSAN QX60 HYBRID, MURANO HYBRID, PATHFINDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E087000·2021-10-01

    Arcimoto Recalls TRiO Conversion Kits Due to Bolt Failure Risk

    Arcimoto is recalling TRiO conversion kits because a connecting bolt may fail, causing immediate loss of traction power and increasing crash risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V770000·2021-10-01

    2021 Ford Bronco Passenger Air Bag Vent Deployment Defect

    Ford is recalling certain 2021 Bronco vehicles because the passenger air bag vent may open prematurely during deployment, increasing the risk of injury during a crash.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V771000·2021-10-01

    Mercedes-Benz Recalls 2020 GLS 580 Vehicles Due to Air Bag Software Defect

    Mercedes-Benz is recalling 2020 GLS 580 vehicles because incorrect air bag control software may cause the driver's air bag to deploy improperly, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V773000·2021-10-01

    Micro Bird Recalls 2022 G5 School Buses for Wheel Alignment Defect

    Micro Bird is recalling 2022 G5 school buses because misaligned wheels can cause uneven tire wear and increase crash risk. Dealers will re-align the wheels free of charge.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V772000·2021-10-01

    Micro Bird Recalls One 2022 G5 Transit Bus for Wheel Alignment Defect

    Micro Bird is recalling one 2022 G5 transit bus because an incorrectly installed alignment ring can cause wheel misalignment, increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V766000·2021-09-30

    Volvo Recalls S60 and S80 Vehicles for Air Bag Inflator Defect

    Volvo is recalling 2001-2009 S60 and 2001-2006 S80 vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    VOLVO — VOLVO S60, S80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V762000·2021-09-30

    Jayco Recalls 2021-2022 Flight SLX Trailers Due to Fire Risk

    Jayco is recalling 2021-2022 Flight SLX travel trailers because the cooktop may not be sealed from the furnace, creating a fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V764000·2021-09-30

    Highland Ridge RV Recalls 2021 Open Range Trailers Due to Fire Risk

    Highland Ridge RV is recalling 2021 Open Range recreational trailers because the cooktop cabinet may not be sealed from the furnace, creating a fire risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V763000·2021-09-30

    2021-2022 Starcraft Autumn Ridge Outfitter cooktop fire hazard

    Starcraft is recalling 2021-2022 Autumn Ridge Outfitter recreational trailers because the cooktop may invert during furnace operation, increasing fire risk. Dealers will install sealant and plywood panels free of charge.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AUTUMN RIDGE OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2480-2021·2021-09-29

    Ultrasound Gels and Lotions Recalled Due to Bacterial Contamination

    Eco-Med Pharmaceutical, Inc. is recalling ultrasound gels and lotions that may contain bacterial contamination. Products were distributed nationally and internationally.

    Product
    EcoGel 100 Imaging Gel, EcoGel 200 MultiPurpose Gel (Blue), EcoGel 200 MultiPurpose Gel (CLEAR), and EcoLotion Transmission Lotion 1) 100, 200 gel Intended for use in acoustic coupling of ultrasound transducer to tissue 2) Lotion Ecolotion transmission and massage lotion is…
    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
  • SevereFDA (Drugs)·D-0820-2021·2021-09-29

    Fulvestrant Injection Recall: Lack of Sterility Assurance

    Glenmark Pharmaceuticals is recalling Fulvestrant Injection 250 mg/5 mL due to lack of assurance of sterility. The affected product was distributed nationwide in 28,658 cartons across multiple lots.

    Product
    FULVESTRANT — FULVESTRANT (FULVESTRANT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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 (Drugs)·D-0819-2021·2021-09-29

    X Rated Honey For Men Recalled for Undisclosed Tadalafil

    Phe Inc is recalling X Rated Honey For Men packets nationwide because the product contains Tadalafil and was marketed without FDA approval. Consumers should stop use immediately.

    Product
    X RATED HONEY FOR MEN, packaged in 15g packets, 4 packets per box, UPC 6 13682 41232 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2515-2021·2021-09-29

    Univation X System Knee Implant Devices Recalled for Loosening Risk

    Aesculap Implant Systems is recalling Univation X System knee implant devices because they may loosen, potentially requiring revision surgery. All lots distributed in the US are affected.

    Product
    Univation X System knee implant devices as follows: Catalog/Product: NO180Z AS UNIVATION XF FEMUR CEMENTED F1 RM; NO181Z AS UNIVATION XF FEMUR CEMENTED F2 RM; NO182Z AS UNIVATION XF FEMUR CEMENTED F3 RM; NO183Z AS UNIVATION XF FEMUR CEMENTED F4 RM; NO184Z AS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2539-2021·2021-09-29

    SureStep Foley Catheter Tray Recalled for Sterile Barrier Packaging Defect

    C.R. Bard Inc is recalling approximately 4830 SureStep Foley catheter trays due to potential packaging defects that could compromise the sterile barrier.

    Product
    Catalog A902416, SureStep" Foley Tray, Silicone, Urine Meter, StatLock" Stabilization Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2514-2021·2021-09-29

    Univation X System Knee Implants Recalled for Loosening Risk

    Aesculap Implant Systems recalls Univation X System knee implants nationwide due to risk of loosening that could require revision surgery. All lots are affected.

    Product
    Univation X System knee implant devices as follows: Catalog/Product: NO156Z AS UNIVATION XF TIBIA CEMENTED T1 RM; NO157Z AS UNIVATION XF TIBIA CEMENTED T2 RM; NO158Z AS UNIVATION XF TIBIA CEMENTED T3 RM; NO159Z AS UNIVATION XF TIBIA CEMENTED T4 RM; NO160Z AS…
    Category
    Medical Device
    Distribution
    Distributed nationwide