State

Kansas product recalls

73,738 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,821
Critical: 1,053
Severe: 1,485
Most recent: 2026-10-28

Of the 5,821 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,485 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35151–35175 of 79559

SevereFDA (Drugs)·D-1676-2019·2019-08-14
RXQ Compounding Recalls Manganese Sulfate Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Manganese Sulfate Monohydrate Injection because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.
Product
MANGANESE SULFATE MONOHYDRATE (PFV) 0.1MG/ML INJ, 10 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0952-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1694-2019·2019-08-14
RXQ Compounding Recalls Potassium Chloride Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Potassium Chloride 15% Injection Solution due to a lack of assurance of sterility. The recall covers all lots within expiry distributed nationwide.
Product
POTASSIUM CHLORIDE 15% (2MEQ/ML) INJ SOLN, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0954-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1657-2019·2019-08-14
RXQ Compounding Recalls Epinephrine Syringes Due to Sterility Concerns
RXQ Compounding LLC is recalling Epinephrine 1:1000 Injection Solution syringes because the company cannot ensure the product is sterile.
Product
EPINEPHrine 1:1000 INJECTION SOLUTION (PF) Syringe, 1 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0947-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2168-2019·2019-08-14
Centurion Medical Recalls High Drainage LVAD Tray Kits Due to Packaging Concerns
Centurion Medical Products Corporation is recalling 192 High Drainage LVAD Tray Kits because sterile packaging may be compromised.
Product
HIGH DRAINAGE LVAD TRAY Kit Code: DM950 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient population.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1685-2019·2019-08-14
RXQ Compounding Recalls Molybdenum Injection Solution Due to Sterility Concerns
RXQ Compounding LLC is recalling Molybdenum 0.025mg/mL Injection Solution because the product lacks assurance of sterility.
Product
MOLYBDENUM 0.025MG/ML INJECTION SOLUTION, 10ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0964-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1656-2019·2019-08-14
RXQ Compounding Recalls Epinephrine Infusion Bags Due to Sterility Concerns
RXQ Compounding LLC is recalling Epinephrine 4mg in D5W 5% infusion bags because the agency could not ensure the product was sterile.
Product
EPINEPHrine 4MG ADDED TO D5W 5%, 250 ML per bag, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0113-22
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1718-2019·2019-08-14
RXQ Compounding Recalls Zinc Sulfate Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Zinc Sulfate 1mg/mL Injection Solution because the product lacks assurance of sterility.
Product
ZINC SULFATE 1MG/ML INJECTION SOLUTION (PFV), 10ML per VIAL, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 70731-0963-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1707-2019·2019-08-14
RXQ Compounding Recalls Sterile Water for Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Sterile Water for Injection USP vials because the product lacks assurance of sterility.
Product
STERILE WATER FOR INJECTION USP, [10, 30, or 50 ML] per Vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 10 ML vial: 70731-0188-10; NDC 30 ML vial: 70731-0188-30; NDC 50 ML vial: 70731-0188-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1973-2019·2019-08-14
FDA Recalls Shirakiku Fish Cake Due to Possible Undeclared Egg, Milk, and Shellfish Contamination
FDA is recalling Shirakiku Fish Cake because it may contain undeclared egg, milk, and shellfish allergens in 20,101 packages distributed across multiple states.
Product
Shirakiku FISH CAKE BOUTEN SK F 20/ 150G, Net Wt. 5.29 oz. Keep Frozen, 7 pcs. UPC 074410925253 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA
Category
Food
Distribution
38 states
SevereFDA (Devices)·Z-2075-2019·2019-08-14
St Jude Medical Recalls 42 Ellipse DR Cardioverter Defibrillators
St Jude Medical is recalling 42 Ellipse DR cardioverter defibrillators due to damaged aluminum wires that may prevent high-voltage therapy delivery.
Product
ELLIPSE DR, Tiered-therapy cardioverter/defibrillator, REF: CD2411-36Q, UDI: 05414734507615
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1692-2019·2019-08-14
RXQ Compounding Recalls Phenylephrine Syringes Due to Sterility Concerns
RXQ Compounding LLC is recalling Phenylephrine HCL 100 mcg/mL syringes because the agency could not ensure the product was sterile.
Product
PHENYLEPHRINE HCL 100 MCG/ML IN NACL 0.9% SYR, 10 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0136-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1717-2019·2019-08-14
RXQ Compounding Recalls Vitamin B Complex 100 Due to Sterility Concerns
RXQ Compounding LLC is recalling Vitamin B Complex 100 vials because the product may lack assurance of sterility.
Product
VITAMIN B COMPLEX 100 (PFV), [2 or 30 ML] per Vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 2 ML Vial: 70731-0961-02; NDC 30 ML Vial: 70731-0961-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1663-2019·2019-08-14
RXQ Compounding Recalls Glutathione Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Glutathione 200mg/mL Injection Solution because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.
Product
GLUTATHIONE 200MG/ML (MDV) INJECTION SOLN, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0906-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1653-2019·2019-08-14
RXQ Compounding Recalls EDETATE DISODIUM 15% INJECTABLE Due to Sterility Concerns
RXQ Compounding LLC is recalling EDETATE DISODIUM 15% INJECTABLE, 100 ML vials, because the product lacks assurance of sterility.
Product
EDETATE DISODIUM 15% INJECTABLE, 100 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0922-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1687-2019·2019-08-14
RXQ Compounding Recalls Moxifloxacin Ophthalmic Solution Due to Sterility Concerns
RXQ Compounding LLC is recalling Moxifloxacin 0.5% Ophthalmic Solution syringes because the product lacks assurance of sterility.
Product
MOXIFLOXACIN 0.5% OPHTH SOLUTION SYRINGE, 1 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0973-81
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1711-2019·2019-08-14
RXQ Compounding Recalls Travasol 10% Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Travasol 10% Injection Solution because the product lacks assurance of sterility.
Product
TRAVASOL 10% (AMINO ACID) INJECTION SOLUTION, 50 ML per Vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 70731-0151-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1719-2019·2019-08-14
RXQ Compounding Recalls Zinc Sulfate Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling Zinc Sulfate 1mg/mL Injection Solution because the product lacks assurance of sterility.
Product
ZINC SULFATE 1MG/ML INJECTION SOLUTION, 30ML per VIAL, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 70731-0152-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V598000·2019-08-14
E-One Fire Trucks Recalled for Front Shock Separation Risk
E-One is recalling specific Typhoon, Quest, and Cyclone II fire trucks because front shocks may separate, potentially damaging steering components and increasing crash risk.
Product
E-ONE — E-ONE TYPHOON, QUEST, CYCLONE II
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1655-2019·2019-08-14
RXQ Compounding Recalls Ephedrine Syringes Due to Sterility Concerns
RXQ Compounding LLC is recalling Ephedrine 5mg/mL syringes nationwide because the product lacks assurance of sterility.
Product
EPHEDRINE 5MG/ML (PF) SYRINGE, 5 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0201-85
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1658-2019·2019-08-14
FDA Recalls Fentanyl Injection Due to Sterility Assurance Concerns
RXQ Compounding LLC is recalling fentanyl injection syringes because the agency could not ensure the product was sterile.
Product
fentaNYL 0.05MG/ML INJ SOL (PF), 55ML per syringe (C-II) RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0118-55
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1700-2019·2019-08-14
RXQ Compounding Recalls Pyridoxine Vials Due to Sterility Concerns
RXQ Compounding LLC is recalling Pyridoxine (PFV) 100mg/mL vials because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.
Product
PYRIDOXINE (PFV) 100MG/ML, 30ML PER VIAL. RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0955-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2219-2019·2019-08-14
Ideal Implant Recalls Structured Saline Breast Implants Due to Deflation
Ideal Implant Incorporated is recalling 1,704 structured saline breast implants because a silicone piece disrupted the valve seal, causing deflation shortly after implantation.
Product
IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc, 335cc, 370cc, 405cc, 440cc, 475cc, 515cc, 555cc, 595cc, 635cc, and 675cc.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1712-2019·2019-08-14
RXQ Compounding Recalls Turbo Caine 2.5 Due to Sterility Concerns
RXQ Compounding LLC is recalling Turbo Caine 2.5 syringes because the FDA determined there is a lack of assurance of sterility.
Product
TURBO CAINE 2.5 (PHEN2.5/CYCLO1/ TROP1/TETRA 0.5), 0.4 ML per Syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 70731-0193-81
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1706-2019·2019-08-14
RXQ Compounding Recalls SOD-PHOS Injection Due to Sterility Concerns
RXQ Compounding LLC is recalling SOD-PHOS injection vials because the product lacks assurance of sterility. The recall covers all lots within their expiry dates.
Product
SOD-PHOS (PHOS 3MMOL/ML-SOD 4MEQ/ML) PFV INJ SOLN, 10 ML PER VIAL, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0905-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2070-2019·2019-08-14
St Jude Medical Recalls 27 Ellipse VR Implantable Cardioverter Defibrillators
St Jude Medical is recalling 27 Ellipse VR implantable cardioverter defibrillators due to damaged aluminum wires that may prevent the delivery of high-voltage therapy.
Product
ELLIPSE VR, REF: CD1377-36C Implantable cardioverter defibrillators (ICDs)
Category
Medical Device
Distribution
Distributed nationwide