Wyoming recalls
3250 federal recalls on file affecting Wyoming - 173 Wyoming-specific plus 3077 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-11-05FDA-DrugFarmakeio OutsourcingClass IINationwideTestosterone 200 MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0381-01
CGMP Deviations: Potential presence of metal particulate matter
- 2025-11-05FDA-DrugFarmakeio OutsourcingClass IINationwideTestosterone 87.5 MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0386-01
CGMP Deviations: Potential presence of metal particulate matter
- 2025-11-05FDA-DrugFarmakeio OutsourcingClass IINationwideTestosterone 62.5 MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0383-01
CGMP Deviations: Potential presence of metal particulate matter
- 2025-11-05FDA-DrugFarmakeio OutsourcingClass IINationwideTestosterone 50MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0387-01
CGMP Deviations: Potential presence of metal particulate matter
- 2025-11-05FDA-DrugFarmakeio OutsourcingClass IINationwideTestosterone 25MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0389-01
CGMP Deviations: Potential presence of metal particulate matter
- 2025-11-05FDA-DrugAcmeClass IINationwideSting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001, Manufactured for: Acme United Corporation, 1 Waterview Dr. Shelton, CT, Made in the USA UPC 738743190015
Product Mix-up
- 2025-11-05FDA-DrugKenvueClass IINationwideTYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division, Fort Washington, PA 19034, NDC: 50580-378-04.
Defective Container
- 2025-11-05FDA-DrugQuVa PharmaClass IINationwideR.E.C.K. (Ropivacaine HCl, EPINEPHrine, CloNIDine HCl, and Ketorolac Tromethamine) in Sodium Chloride Solution, Total Volume: 50 mL syringe. INJECTION FOR PERIARTICULAR USE; Not for IV Use. THIS IS A COMPOUNDED DRUG. QuVA Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, TX 77478. NDC 70092-1433-50
Presence of Particulate Matter
- 2025-11-05FDA-DrugHeritage PharmaceuticalsClass IINationwideDesipramine Hydrochloride Tablets, USP, 150 mg, 50 count bottle (NDC 23155-583-25), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- 2025-11-05FDA-DrugHeritage PharmaceuticalsClass IINationwideDesipramine Hydrochloride Tablets, USP, 100 mg, 100 count bottle (NDC 23155-582-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- 2025-11-05FDA-DrugHeritage PharmaceuticalsClass IINationwideDesipramine Hydrochloride Tablets, USP, 75 mg, 100 count bottle (NDC 23155-581-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- 2025-11-05FDA-DrugHeritage PharmaceuticalsClass IINationwideDesipramine Hydrochloride Tablets, USP, 50 mg, 100 count bottle (NDC 23155-580-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- 2025-11-05FDA-DrugHeritage PharmaceuticalsClass IINationwideDesipramine Hydrochloride Tablets, USP, 25 mg, 100 count bottle (NDC 23155-579-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- 2025-11-05FDA-DrugHeritage PharmaceuticalsClass IINationwideDesipramine Hydrochloride Tablets, USP, 10 mg, 100 - count bottle (NDC 23155-578-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- 2025-11-05FDA-DrugTevaClass IINationwidePrazosin Hydrochloride, Capsules, USP, 5 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4069-01, b) 250 Capsules, NDC 0093-4069-52, c) 500 Capsules, NDC 0093-4069-05
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
- 2025-11-05FDA-DrugTevaClass IINationwidePrazosin Hydrochloride, Capsules, USP, 2 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4068-01, b) 1000 Capsules, NDC 0093-4068-10
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
- 2025-11-05FDA-DrugTevaClass IINationwidePrazosin Hydrochloride, Capsules, USP, 1 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4067-01, b) 1000 Capsules, NDC 0093-4067-10
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
- 2025-11-05FDA-DrugAmerisourceClass IINationwidePrazosin Hydrochloride, Capsules, USP, 5 mg, 20 capsules (5x4) cartons, Rx only, Distributed by American Health Packaging, Columbus, Ohio 43217, carton NDC 60687-572-32, Individual unit dose: NDC 60687-572-33
Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit
- 2025-11-05FDA-DrugAmerisourceClass IINationwidePrazosin Hydrochloride, Capsules, USP, 2 mg, 100 capsules (10x10) cartons, Rx only, Distributed by American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-997-01, Individual unit dose: NDC 68084-997-11
Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit
- 2025-11-05FDA-DrugAmerisourceClass IINationwidePrazosin Hydrochloride, Capsules, USP, 1 mg, 100 capsules (10x10) cartons, Rx only, Distributed by American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-996-01. Individual unit dose: NDC 68084-996-11
Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit
- 2025-11-05FDA-DrugBreckenridgeClass IINationwideDuloxetine Delayed-Release Capsules, USP, 60 mg, a.) 90-count bottle (NDC: 51991-748-90), b.)1000-count bottle (NDC 51991-748-10),Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain; Dist. by: Breckenridge Pharmaceutical, Inc., Berkeley Heights, NJ 07922.
CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment limit of 12.5ppm.
- 2025-11-04USDAClass INationwideThrow out Brazilian Taste croquettes (sesame allergen)
Misbranding, Unreported Allergens
- 2025-10-30CPSCJiangsu Zhi Pai FurnitureNationwideWLIVE Fabric Drawer Dressers Recall Expanded to Include 16-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units; Sold on Amazon by WLIVE
The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- 2025-10-30CPSCCarole AccessoriesNationwideThe Kroger Co. Recalls Halloween-Themed Skeleton Wax Candles Due to Fire Hazard
The candle contains ornaments that are flammable, posing fire and burn hazards.
- 2025-10-30CPSCMilwaukeeNationwideMilwaukee Tool Recalls M18 FUEL 14" and 12" Top Handle Chainsaws Due to Laceration Hazard
The recalled chainsaw's chain brake may not activate, posing a laceration hazard.
- 2025-10-30CPSCDINBooonLUXNationwideDINBooonLUX 12-Inch Full Size Mattresses Recalled Due to Risk of Serious Injury or Death from Fire; Violates Mandatory Standard for Mattress Flammability; Sold on Amazon by DINBooonLUX
The mattresses violate the mandatory flammability standard, posing a risk of serious injury or death from fire.
- 2025-10-30CPSCChampionNationwideAvenco and Novilla Mattresses Recalled Due to Risk of Serious Injury or Death from Fire; Violates Mandatory Flammability Standard for Mattresses; Manufactured by PT Champion
The mattresses violate mandatory flammability standards for mattresses, posing a risk of serious injury or death from fire.
- 2025-10-30CPSCHarppaNationwide5-in-1 Convertible High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violates Mandatory Standard for High Chairs; Imported by Harppa
The high chairs pose a risk of serious injury or death to children because they violate the mandatory standard for high chairs. The high chairs were sold without the required attached restraint system, posing a serious risk of falls to children. In addition, a child's head can become trapped in the opening created between the seat and the tray, posing a deadly entrapment hazard.
- 2025-10-30CPSCHOMEALNationwideHOMEAL Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment; Violates Mandatory Standard for Children's Portable Bed Rails; Sold on Amazon by HOMEAL
The recalled bed rails violate the mandatory standard for children's portable bed rails because when installed adjacent to the bed, a child can become entrapped in the openings on the side of the mattress, posing a risk of serious injury or death due to entrapment.
- 2025-10-30CPSCCrate and BarrelNationwideCrate & Barrel Recalls Ana Dining Chairs Due to Fall Hazard
The legs of the dining chair can break, posing a fall hazard.
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