The Recall Desk

State

Wyoming product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24351–24375 of 76822

  • ModerateFDA (Drugs)·D-0774-2021·2021-09-08

    Cyclobenzaprine Hydrochloride Tablets 7.5mg Recalled for Microbial Contamination

    Teva Pharmaceuticals is recalling Cyclobenzaprine Hydrochloride Tablets 7.5mg due to out-of-specification microbial counts in an ingredient batch. The product was distributed nationwide.

    Product
    Cyclobenzaprine Hydrochloride Tablets, 7.5mg, 100 count tablets per bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 0591-3330-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0787-2021·2021-09-08

    Clopidogrel Tablets Recalled for Foreign Matter Contamination

    Macleods Pharma USA is recalling Clopidogrel 75 mg tablets due to the presence of foreign matter in the product. The affected lot was distributed nationwide.

    Product
    CLOPIDOGREL — CLOPIDOGREL (CLOPIDOGREL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2393-2021·2021-09-08

    Steripath Luer Transport Pack Gen2 Recalled for Incorrect Instructions

    Magnolia Medical Technologies is recalling 9,400 units of Steripath Luer Transport Pack Gen2 because they were shipped with incorrect Transfer Adapter Instructions For Use (IFU).

    Product
    Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer¿ Blood Collection or Urine Collection Tubes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2407-2021·2021-09-08

    COVID-19 diagnostic test distributed outside certified laboratory channels

    CareStart COVID-19 Antigen Rapid Diagnostic Test units were distributed to non-CLIA-certified customers, violating the product's Emergency Use Authorization requirements.

    Product
    CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals suspected of COVID-19 by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0785-2021·2021-09-08

    Lidocaine Ointment USP 5% Recalled for Failed Viscosity Specifications

    Teligent Pharma is recalling Lidocaine Ointment USP 5% (114,456 tubes, Lots 15378 and 14418) distributed nationwide because certain lots do not meet viscosity specifications, as determined through routine testing.

    Product
    Lidocaine Ointment USP, 5% Rx Only, Net Wt 35.44 g(1 1/4 oz)packaged in a laminat tube, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-008-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0784-2021·2021-09-08

    Donepezil HCL Tablets 5 mg Recalled for Subpotency

    Jubilant Cadista Pharmaceuticals is recalling Donepezil HCL Tablets, USP, 5 mg (Lot # DN120006A, exp. 12/2021) because the tablets are subpotent—meaning they contain less active ingredient than specified. The recall affects 14,544 bottles distributed nationwide.

    Product
    Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. India, Marketed by: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801 NDC 59746-329-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V694000·2021-09-07

    Eldorado EZRM Recalled for Fuel Hose Leak Fire Risk

    Eldorado National is recalling 2019-2021 EZRM vehicles with L9 Diesel Engines due to a fuel hose leak that increases fire risk.

    Product
    ELDORADO — ELDORADO EZRM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V693000·2021-09-07

    LDJ Recalls 2021 Thunder Creek Trailers Due to Fender Light Wiring Defect

    LDJ Manufacturing is recalling 279 2021 Thunder Creek trailers because improperly routed wiring may cause fender clearance lights to fail, increasing crash risk.

    Product
    THUNDER CREEK — THUNDER CREEK STT, MTO, SLT, MTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E084000·2021-09-04

    Nineo F2-H11 LED Bulbs Recalled for Excessive Brightness

    Nineo is recalling F2-H11 replacement LED bulbs because they may be too bright, posing a glare hazard to oncoming drivers.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V691000·2021-09-03

    2021 Forest River Berkshire RVs Recalled for Electrical Fire Risk

    Forest River is recalling certain 2021 Berkshire recreational vehicles that may have unsealed mini-breakers in the electrical system, which could cause sparks and increase the risk of fire in the battery compartment.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V692000·2021-09-03

    2021-2022 Coachmen Nova motorhomes recalled for improper battery installation

    Forest River is recalling 2021-2022 Coachmen Nova motorhomes because the Absorbed Glass Mat battery was incorrectly installed, allowing hydrogen gas to accumulate inside the vehicle and create a risk of injury.

    Product
    COACHMEN — COACHMEN NOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V686000·2021-09-02

    Highland Ridge RV Recalls 1,157 Units Due to Propane Regulator Failure

    Highland Ridge RV is recalling 1,157 recreational vehicles because a propane regulator may fail, causing increased pressure and fire risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW OPEN RANGE, OPEN RANGE ULTRA LITE, OPEN RANGE LIGHT, SILVERSTAR LIMITED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V688000·2021-09-02

    Toyota Tundra vehicles recalled due to headlight electrical circuit fire risk

    Certain 2018-2021 Toyota Tundra vehicles have a headlight electrical circuit defect that may power high and low beams simultaneously, causing connector overheating and fire risk. Owners should contact Toyota or NHTSA for remedy information.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21778·2021-09-02

    Step2 StepUp Sidekick Learning Towers Recalled Due to Fall Hazard

    The Step2 Company is recalling StepUp Sidekick Learning Towers because the storage tray with cup holders and step can come loose, posing a fall hazard to children. Step2 has received 20 reports of the component coming loose, including one report of minor bruises from a fall.

    Product
    StepUp Sidekick Learning Towers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V689000·2021-09-02

    Freightliner Cascadia trucks recalled for potential steering linkage separation

    Daimler Trucks North America is recalling 2019-2021 Freightliner Cascadia trucks due to improperly tightened drag link taper joints that could separate from the steering arm. Loss of steering control could result, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V681000·2021-09-02

    Indian Recalls 2020 Scout Bobber Sixty for Inoperable Brake Lights

    Indian Motorcycle is recalling 2020 Scout Bobber Sixty models because an ECU update may have disabled brake lights, increasing crash risk.

    Product
    INDIAN — INDIAN SCOUT BOBBER SIXTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V687000·2021-09-02

    2021 Starcraft Telluride RV Propane Regulator Failure Fire Risk

    Starcraft is recalling certain 2021-2022 recreational vehicles with defective Winntec propane regulators that may fail, causing increased pressure and larger flames in gas appliances, raising fire risk.

    Product
    STARCRAFT RV FW — STARCRAFT RV FW, STARCRAFT RV TT TELLURIDE, SUPER LITE, AUTUMN RIDGE OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V685000·2021-09-02

    Jayco Recreational Vehicles Recalled for Propane Regulator Fire Risk

    Jayco is recalling certain 2017-2022 recreational vehicles with Winntec propane regulators that may fail and increase propane pressure, raising the risk of fire in gas appliances.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER, JAYCO SEISMIC, JAY FLIGHT BUNGALOW, EAGLE, JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2285-2021·2021-09-01

    Monoject Sodium Chloride Flush Syringes Recalled for Air Embolism Risk

    Cardinal Health recalls 267 million Monoject 0.9% Sodium Chloride Flush Syringes due to a plunger defect that may reintroduce air into the syringe, posing a risk of air embolism during IV administration.

    Product
    Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0765-2021·2021-09-01

    Fludarabine Phosphate Injection Recalled Due to Sterility Concern

    Custopharm, Inc. is recalling Fludarabine Phosphate for Injection, USP 50 mg because the manufacturer detected microbial contamination during environmental monitoring in aseptic manufacturing areas, raising sterility assurance concerns.

    Product
    FLUDARABINE PHOSPHATE FOR INJECTION, USP, 50 mg per vial, Single dose vial, Rx Only, Mfd for: Leucadia Pharmaceuticals Carlsbad, CA 92011 U.S.A, NDC 24201-237-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2286-2021·2021-09-01

    Sodium Chloride Flush Syringe Recalled Due to Plunger Malfunction Risk

    Cardinal Health is recalling Monoject 0.9% Sodium Chloride Flush Syringes because the plunger may draw back after use and reintroduce air into the syringe.

    Product
    Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0768-2021·2021-09-01

    SterRx Sodium Bicarbonate in 5% Dextrose Injection Recalled for Sterility Concerns

    SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection (1,000 mL bags) nationwide due to lack of assurance of sterility. Patients using affected lots should consult their healthcare provider immediately.

    Product
    Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0767-2021·2021-09-01

    SterRx Sodium Bicarbonate Injection Recalled for Non-Sterility

    SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection due to microbial contamination confirmed by third-party laboratory testing. The affected product is a prescription intravenous injection distributed nationwide.

    Product
    Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903 NDC 70324-326-01
    Category
    Drug
    Distribution
    Distributed nationwide