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.

54476–54500 of 79655

ModerateFDA (Drugs)·D-0605-2016·2016-02-03
Pharmakon Recalls Provocholine Pre-diluted Sets Due to Stability Data Concerns
Pharmakon Pharmaceuticals is recalling 378 units of Provocholine Pre-diluted Set II because stability data does not support the expiration dates. The recall covers lots expiring up to November 17, 2015.
Product
Provocholine Pre-diluted Set II in 0.9% Sodium Chloride, 16 mg/mL, 3 mL in 5 mL Syr, injectable packed in syringes, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateNHTSA·16V059000·2016-02-03
Forest River Recalls 2016 Wildcat Trailers for Incorrect Weight Placards
Forest River is recalling 52 model year 2016 Wildcat recreational trailers because they may have incorrect Federal placards with a reduced Gross Axle Weight Rating.
Product
FOREST RIVER — FOREST RIVER WILDCAT
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0599-2016·2016-02-03
Pharmakon Recalls Glycopyrrolate Syringes Due to Stability Data Concerns
Pharmakon Pharmaceuticals is recalling 1,530 syringes of Glycopyrrolate 0.2 mg/mL because stability data does not support the expiration dates.
Product
Glycopyrrolate 0.2 mg/mL, injectable packed in syringes, Total dosage 1 mg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0610-2016·2016-02-03
Amerisource Recalls Levofloxacin Tablets Due to Dissolution Failures
Amerisource Health Services is recalling 3,888 cartons of Levofloxacin 500 mg tablets because they failed dissolution specifications.
Product
Levofloxacin Tablets USP, 500 mg, packaged in 100-count (10 x 10) blister cards per carton, individual blisters labeled UPC (01) 003 68084 482 11 3, carton labeled NDC 68084-482-01, UPC (01) 0 03 68084 482 01 4; Rx only, Packaged and Distributed by: American Health Packaging…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0602-2016·2016-02-03
Pharmakon Recalls Ketamine Syringes Due to Insufficient Stability Data
Pharmakon Pharmaceuticals is recalling 250 syringes of Ketamine 50 mg/mL because stability data does not support the expiration dates.
Product
Ketamine 50 mg/mL, injectable packed in syringes, Total dosage 50 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0594-2016·2016-02-03
Pharmakon Recalls Ondansetron Syringes Due to Insufficient Stability Data
Pharmakon Pharmaceuticals is recalling 4,100 units of Ondansetron 2 mg/mL injectable syringes because stability data does not support the expiration dates.
Product
Ondansetron 2 mg/mL, injectable packed in syringes, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0588-2016·2016-02-03
Pharmakon Recalls Ephedrine Sulfate Syringes Due to Stability Data Issues
Pharmakon Pharmaceuticals is recalling Ephedrine Sulfate 5 mg/mL injectable syringes because stability data does not support the expiration dates.
Product
Ephedrine Sulfate 5 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 25 mg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0595-2016·2016-02-03
Pharmakon Recalls Midazolam Syringes Due to Insufficient Stability Data
Pharmakon Pharmaceuticals is recalling 665 syringes of Midazolam (PF) because stability data does not support the expiration dates. The recall is nationwide.
Product
Midazolam (PF) 0.1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 0.2 mg/ 2mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0596-2016·2016-02-03
Pharmakon Recalls Fentanyl Citrate Syringes Due to Stability Data Issues
Pharmakon Pharmaceuticals is recalling Fentanyl Citrate syringes because stability data does not support the expiration dates. The recall covers 7,100 units distributed nationwide.
Product
Fentanyl Citrate (PF) 50 mcg/mL, injectable packed in syringes a) Total dosage 250 mcg/ 5mL, b) Total dosage 100 mcg/ 2mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0697-2016·2016-02-03
Phadia Recalls EliA SmDP Wells Due to Invalid Test Results
Phadia Ab is recalling 76 units of EliA SmDP Well lot 0018 because nonspecific signals may cause incorrect positive or equivocal test results for systemic lupus erythematosus.
Product
EliA SmDP Well, Article Number 14-5624-01 Product Usage: EliA SmDP is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to Sm in human serum and plasma (EDTA, citrate) as an aid in the clinical diagnosis of systemic lupus erythematosus (SLE)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0587-2016·2016-02-03
Perrigo Recalls Children's Guaifenesin DM Liquid Due to Dosing Cup Errors
Perrigo is recalling specific lots of Children's Guaifenesin DM Cherry liquid because the included dosing cups have incorrect dose markings.
Product
Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan HBr 5 mg/5 mL), packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold under the following: a) Sunmark, Children's Mucus Relief Cough, Guaifenesin 100 mg/Expectorant…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0606-2016·2016-02-03
Pharmakon Recalls Provocholine Pre-diluted Sets Due to Stability Data Issues
Pharmakon Pharmaceuticals is recalling Provocholine Pre-diluted Set II because stability data does not support the expiration dates. All lots expiring up to 11/17/2015 are affected.
Product
Provocholine Pre-diluted Set II in 0.9% Sodium Chloride, 4 mg/mL, 3 mL in 5 mL Syr, injectable packed in syringes, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0604-2016·2016-02-03
Pharmakon Recalls Lidocaine HCI Injectable Syringes Due to Stability Data
Pharmakon Pharmaceuticals is recalling Lidocaine HCI 2% injectable syringes because stability data does not support the expiration dates.
Product
Lidocaine HCI (PF) Inj, USP 2%, injectable packed in syringes, Total dosage 100 mg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0603-2016·2016-02-03
Pharmakon Recalls Midazolam Syringes Due to Insufficient Stability Data
Pharmakon Pharmaceuticals is recalling 5,000 syringes of Midazolam 1 mg/mL because stability data does not support the expiration dates.
Product
Midazolam 1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 2 mg/ 2mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0609-2016·2016-02-03
Pharmakon Recalls Provocholine Pre-diluted Sets Due to Stability Data Issues
Pharmakon Pharmaceuticals is recalling Provocholine Pre-diluted Set II because stability data does not support the expiration dates. The recall covers all lots expiring through November 17, 2015.
Product
Provocholine Pre-diluted Set II in 0.9% Sodium Chloride, 0.0625 mg/mL, 3 mL in 5 mL Syr, injectable packed in syringes, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0586-2016·2016-02-03
Perrigo Recalls Guaifenesin Liquid Due to Incorrect Dosing Cup Markings
Perrigo Company PLC is recalling specific lots of Guaifenesin liquid because the included dosing cups have incorrect dose markings.
Product
Guaifenesin Grape liquid 100 mg/5 mL, packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold under the following: a) H.E.B. Mucus Relief, Children's Guaifenesin, Expectorant, Age 4+, Grape Flavor, Gluten Free, Alcohol Free, 4 FL OZ (118 mL) Bottle, Made…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0597-2016·2016-02-03
Pharmakon Recalls Morphine Sulfate Syringes Due to Stability Data Concerns
Pharmakon Pharmaceuticals is recalling 475 syringes of Morphine Sulfate (PF) 0.5 mg/mL because stability data does not support the expiration dates.
Product
Morphine Sulfate (PF) 0.5 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 0.5 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0600-2016·2016-02-03
Pharmakon Recalls Ketamine Syringes Due to Insufficient Stability Data
Pharmakon Pharmaceuticals is recalling 600 syringes of Ketamine 100 mg/mL because stability data does not support the expiration dates.
Product
Ketamine 100 mg/mL, injectable packed in syringes, Total dosage 100 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0647-2016·2016-02-03
Bausch & Lomb Recalls Tropicamide Ophthalmic Solution Due to Labeling Error
Bausch & Lomb is recalling Tropicamide Ophthalmic Solution because the package insert is missing updates compared to the reference drug insert.
Product
TROPICAMIDE — TROPICAMIDE (TROPICAMIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0645-2016·2016-02-03
Bausch & Lomb Recalls Cyclopentolate Hydrochloride Ophthalmic Solution for Labeling Errors
Bausch & Lomb is recalling Cyclopentolate Hydrochloride Ophthalmic Solution 1% because the package insert is missing updates compared to the reference drug insert.
Product
CYCLOPENTOLATE HYDROCHLORIDE — CYCLOPENTOLATE HYDROCHLORIDE (CYCLOPENTOLATE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0646-2016·2016-02-03
Bausch & Lomb Recalls Tropicamide Ophthalmic Solution Due to Labeling Defect
Bausch & Lomb is recalling Tropicamide Ophthalmic Solution 0.5% because the package insert is missing updates compared to the reference drug insert.
Product
TROPICAMIDE — TROPICAMIDE (TROPICAMIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V056000·2016-02-02
Honda Recalls 2008-2010 Accord Vehicles Due to Air Bag Control Unit Defect
Honda is recalling 2008-2010 Accord vehicles because air bag control units may corrode and fail, potentially preventing air bags from deploying in a crash.
Product
HONDA — HONDA ACCORD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V058000·2016-02-02
Highland Ridge RV Recalls Travel Trailers With Underrated Safety Chains
Highland Ridge RV is recalling 2015-2016 travel trailers because the safety chains are rated for less weight than the trailers' gross vehicle weight rating.
Product
HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ROAMER, HIGHLANDER, MESA RIDGE, JOURNEYER
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·16089·2016-02-02
Microsoft Recalls Surface Pro AC Power Cords Due to Fire and Shock Hazards
Microsoft is recalling approximately 2.25 million AC power cords for Surface Pro devices because they can overheat, posing fire and electrical shock risks.
Product
AC Power cords
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·16V055000·2016-02-02
Newmar Recalls 2015-2016 Ventana Motorhomes Due to Rim Pressure Mismatch
Newmar is recalling 2015-2016 Ventana and Ventana LE motorhomes because front rims may have a lower pressure rating than the tires, increasing crash risk.
Product
NEWMAR — NEWMAR VENTANA LE, VENTANA
Category
Vehicle
Distribution
Distributed nationwide