State

Kansas product recalls

73,833 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,053
Severe: 1,486
Most recent: 2026-11-04

Of the 5,822 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 1,486 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55351–55375 of 79655

SevereFDA (Drugs)·D-0287-2016·2015-11-25
US Compounding Recalls Triamcinolone Diacetate Vials Due to Sterility Concerns
US Compounding Inc is recalling 33,778 vials of Triamcinolone diacetate USP PF (40 mg/mL) nationwide due to deficient practices that may impact sterility assurance.
Product
Triamcinolone diacetate USP PF (40 mg/mL), 2 mL Vial, For IM & Regional Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3206-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0248-2016·2015-11-25
US Compounding Recalls Dex LA 8 Vials Due to Sterility Assurance Concerns
US Compounding Inc is recalling 4,333 vials of Dex LA 8 (Dexamethasone acetate) nationwide because deficient practices may have impacted sterility assurance.
Product
Dex LA 8 (Dexamethasone acetate (8 mg/mL), 10 mL Multi-Dose Vial, For IM & Regional Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3299-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0338-2016·2015-11-25
Downing Labs Recalls L-Tyrosine Injectable Due to Sterility Concerns
Downing Labs, LLC is recalling 29 vials of L-Tyrosine Injectable because the product lacks assurance of sterility. The affected product was distributed nationwide and in multiple international markets.
Product
L-Tyrosine Injectable, 25mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0376-2016·2015-11-25
Downing Labs Recalls M.I.C Injection Due to Sterility Concerns
Downing Labs, LLC is recalling M.I.C Injection (Preserved) because the company cannot ensure the product is sterile. The recall affects 172 vials distributed in the US and internationally.
Product
M.I.C Injection (Preserved), 25/50/25mg/mL, 50mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0381-2016·2015-11-25
Downing Labs Recalls Magnesium Sulfate Injection Due to Sterility Concerns
Downing Labs, LLC is recalling 304 vials of Magnesium Sulfate Injection because the product lacks assurance of sterility. The affected vials were distributed nationwide and internationally.
Product
Magnesium Sulfate Injection (4060mOsm/L), 50%, 50mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-335-2016·2015-11-25
Essential Wellness Pharma Recalls TRIMIX #4 Injection Due to Sterility Concerns
Kalman Health & Wellness is recalling TRIMIX #4 Injection vials due to poor sterile production practices that compromise sterility assurance.
Product
TRIMIX #4 (27 mg-1.5 mg-50 mcg/mL) Injection, 5 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0265-2016·2015-11-25
US Compounding Recalls Methylprednisolone Vials Due to Sterility Concerns
US Compounding Inc is recalling 3,629 vials of Methylprednisolone 100 mg/mL due to deficient practices that may impact sterility assurance.
Product
MethylPREDNISolone (100 mg/mL) 10 mL Multi-Dose Vial, For IM & Regional Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3115-07
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-301-2016·2015-11-25
Essential Wellness Pharma Recalls BIMIX INJ Injection Due to Sterility Concerns
Essential Wellness Pharma is recalling BIMIX INJ 30 mg-1 mg/mL Injection vials because poor sterile production practices resulted in a lack of sterility assurance.
Product
BIMIX INJ 30 mg-1 mg/mL Injection, 5 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-311-2016·2015-11-25
Essential Wellness Pharma Recalls HCG Injections Due to Sterility Concerns
Kalman Health & Wellness is recalling HCG 10,000 Units/mL injections because poor sterile production practices created a lack of sterility assurance.
Product
HCG 10,000 Units/mL Injection, packaged in a) 1 mL, b) 1.2 mL, c) 1.6 mL, d) 2.0 mL, e) 2.4 mL, f) 3.6 mL, g) 4 mL, h) 4.8 mL vials; and i) 0.1 mL, j) 0. 2 mL, k) 0.3 mL prefilled syringes, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0368-2016·2015-11-25
Downing Labs Recalls L-Arginine Injection Due to Sterility Concerns
Downing Labs, LLC is recalling L-Arginine Injection, 100mg/mL, 30mL vials because the company cannot assure the sterility of the product.
Product
L-Arginine Injection, 100mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0246-2016·2015-11-25
US Compounding Recalls Cyclopent/PE/Tropic Eye Drops Due to Sterility Concerns
US Compounding Inc is recalling 820 bottles of Cyclopent/PE/Tropic eye drops because deficient practices may have compromised sterility assurance.
Product
Cyclopent/PE/Tropic 2mL (1%/2.5%/0.25%), 2 mL dropper bottles; For topical ophthalmic use, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3299-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0236-2016·2015-11-25
US Compounding Recalls Acetylcysteine 10% Ophthalmic Solution for Sterility Concerns
US Compounding Inc is recalling Acetylcysteine 10% Ophthalmic solution due to deficient practices that may impact sterility assurance.
Product
ACETYLCYSTEINE 10% OPHTALMIC, 10 mL dropper bottle; For topical ophthalmic use, Rx.only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-310-2016·2015-11-25
Essential Wellness Recalls HCG Injection Vials Due to Sterility Concerns
Essential Wellness Pharmacy is recalling HCG 5000 Units/mL injection vials because poor production practices raised concerns about the sterility of the compounded drugs.
Product
HCG 5000 Units/mL Injection, 0.4 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0294-2016·2015-11-25
Fresenius GranuFlo Dissolution Units Recalled for Fire Risk
Fresenius Medical Care is recalling 918 GranuFlo Dissolution Units because they lack full thermal protection, which can generate smoke or lead to fire.
Product
Fresenius 132 Gallon GranuFlo Dissolution Unit - P/N G047-80101. For Use in the Preparation of acid concentrate for hemodialysis.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0279-2016·2015-11-25
US Compounding Recalls Prednisolone Eye Drops Due to Sterility Concerns
US Compounding Inc is recalling Prednisolone Sodium Phosphate eye drops due to deficient practices that may impact sterility assurance.
Product
Prednisolone Sodium Phosphate PF Solution (1%) in 15 mL dropper bottle; For Topical Ophthalmic Use, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72653
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0360-2016·2015-11-25
Downing Labs Recalls Magnesium Sulfate Injectable Due to Sterility Concerns
Downing Labs, LLC is recalling 160 vials of Magnesium Sulfate Injectable because the company cannot assure the sterility of the product.
Product
Magnesium Sulfate Injectable, 14.28%, 7mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0259-2016·2015-11-25
US Compounding Recalls Choline Chloride Inositol Cyanocobalamin Injection Vials
US Compounding Inc is recalling 103 vials of a compounded injection due to deficient practices that may impact sterility assurance.
Product
Choline chloride 50 mg/mL, Inositol 50 mg/mL Cyanocobalamin 1000 mcg/mL, 30 mL Multi-Dose Vial, For Deep IM Injection Only, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3294-06
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0255-2016·2015-11-25
US Compounding Recalls Hyaluronic Acid Syringes Due to Sterility Concerns
US Compounding Inc is recalling 5,118 syringes of Hyaluronic Acid/Lidocaine PF due to deficient practices that may impact sterility assurance.
Product
Hyaluronic Acid/Lidocaine PF (20 mg/1%), 2 mL Single-Use Syringe , For Intra-Articular Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3087-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0372-2016·2015-11-25
Downing Labs Recalls Piracetam Injection Due to Sterility Assurance Concerns
Downing Labs, LLC is recalling Piracetam Injection, 200mg/mL, 10mL vials due to a lack of assurance of sterility. The recall covers all lots distributed nationwide and internationally.
Product
Piracetam Injection, 200mg/mL,10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-332-2016·2015-11-25
Essential Wellness Pharma Recalls TRIMIX #1 Injection Due to Sterility Concerns
Essential Wellness Pharma is recalling TRIMIX #1 Injection vials because poor production practices may have compromised the sterility of the compounded sterile preparations.
Product
TRIMIX #1 Injection, 4.2 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0153-2016·2015-11-25
Kar's Sweet n' Salty Mix Recalled for Possible Glass Contamination
Kar Nut Products Company is recalling 208,008 bags of Kar's Sweet n' Salty Mix due to the possibility of very small pieces of glass in the product.
Product
Kar's Sweet n' Salty Mix 2 oz. flexible film bags. 72 bags per case.
Category
Food
Distribution
36 states
SevereFDA (Devices)·Z-0285-2016·2015-11-25
Prism Medical P-300 Portable Consumer Lift Recalled for Drive Shaft Failure
ErgoSafe Products is recalling 1,721 Prism Medical P-300 Portable Consumer Lifts because the drive shaft and over speed arm may fail, potentially causing a patient to fall.
Product
Prism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051; weight specification 300 lbs. /136 kg.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0292-2016·2015-11-25
US Compounding Recalls Vitamin D3 Vials Due to Sterility Concerns
US Compounding Inc is recalling 55 vials of Vitamin D3 in Olive Oil due to deficient practices that may impact sterility assurance.
Product
Vitamin D3 in Olive Oil (50,000 IU/mL) 30 mL vial, For IM Use only, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3277-06
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0296-2016·2015-11-25
Fresenius Modified Mixer Motor Recalled Due to Fire Risk
Fresenius Medical Care is recalling 992 Modified Mixer Motors for 132 Gallon Dissolution Units because they lack full thermal protection, posing a fire hazard.
Product
Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units), P/N 160075. For Use in the Preparation of acid concentrate for hemodialysis.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0256-2016·2015-11-25
US Compounding Recalls Hyaluronic Acid Syringes Due to Sterility Concerns
US Compounding Inc is recalling 531 hyaluronic acid and lidocaine syringes because deficient practices may have impacted sterility assurance.
Product
Hyaluronic Acid/Lidocaine PF (60 mg/2%), 3 mL Single Use Syringe, For Intra-Articular Injection , Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3249-03
Category
Drug
Distribution
Distributed nationwide