State

Kansas product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37176–37200 of 79562

SevereFDA (Drugs)·D-1020-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine HCl Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 16,075 syringes of Phenylephrine HCl injectable solution nationwide due to a lack of assurance of sterility.
Product
Phenylephrine HCl, 500 mcg in 0.9% Sodium Chloride, QS 5 mL Injectable Solution 500 mcg/5 mL (100 mcg per mL), 5mL Sterile single use syringe, NDC: 42852-830-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1027-2019·2019-03-27
Advanced Pharma Recalls Lidocaine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,980 syringes of 2% Lidocaine HCl Injectable Solution nationwide due to a lack of assurance of sterility.
Product
2% Lidocaine HCl Injectable Solution, 100 mg/5 mL (20 mg per mL), 5mL Sterile single use syringe, NDC: 42852-011-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1018-2019·2019-03-27
Advanced Pharma Recalls Fentanyl Injectable Solution Due to Sterility Concerns
Advanced Pharma Inc. is recalling 180 bags of fentanyl injectable solution nationwide due to a lack of assurance of sterility.
Product
fentaNYL 2500 mcg/250 mL Injectable Solution, Fentanyl 0.9% Sodium Chloride, QS, Sterile single use bags, NDC: 42852-210-25 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1022-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,575 syringes of Phenylephrine HCl injectable solution because the company cannot guarantee the product is sterile.
Product
Phenylephrine HCl, 400 mcg in 0.9% Sodium Chloride, QS 10 mL Injectable Solution 400 mcg/10 mL (40 mcg per mL), Sterile single use syringe, NDC: 42852-876-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1026-2019·2019-03-27
Advanced Pharma Recalls Lidocaine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,540 syringes of 2% Lidocaine HCl Injectable Solution because the company cannot assure the product's sterility.
Product
2% Lidocaine HCl Injectable Solution, 60 mg/3 mL (20 mg per mL), 3mL Sterile single use syringe, NDC: 42852-011-22 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1039-2019·2019-03-27
Shimadzu Mobile X-Ray System Recalled for Brake Failure
Shimadzu is recalling 93 MobileDaRt Evolution mobile X-ray systems because the brakes may fail to engage when the operator releases the drive handle.
Product
SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1065-2019·2019-03-27
Heritage Pharmaceuticals Recalls Subpotent Etomidate Injection Vials
Heritage Pharmaceuticals is recalling 11,888 vials of Etomidate Injection because the drug was found to be subpotent. The recall is voluntary and nationwide.
Product
Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1040-2019·2019-03-27
Fujifilm FDR Go PLUS Mobile X-Ray System Recalled for Braking Defect
Fujifilm is recalling 56 mobile X-ray systems because the braking mechanism may fail to engage when the handle is released.
Product
Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1180-2019·2019-03-27
Best Choice Pancake Mix Recalled for Undeclared Milk Allergen
Gilster-Mary Lee Corp. is recalling Best Choice Pancake & Waffle Complete Mix Original because the product contains milk but the packaging does not declare it as an ingredient.
Product
Best Choice Pancake & Waffle Complete Mix Original 32oz. retail carton, 12 retail units per wholesale case. UPC# 70038 30212
Category
Food
Distribution
5 states
HighNHTSA·19V240000·2019-03-27
Thor Motor Coach Recalls 2018-2020 Models Due to Reversed Backup Camera Image
Thor Motor Coach is recalling 110 motorhomes because the backup camera image may reverse, increasing crash risk. Dealers will install a harness to fix the issue.
Product
THOR MOTOR COACH — THOR MOTOR COACH FOUR WINDS, CHATEAU, MAGNITUDE, OMNI
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1036-2019·2019-03-27
ConvaTec Recalls Feeding Tubes Due to Potential Sterile Barrier Breach
ConvaTec is recalling specific lots of Feeding Tube Metric devices because an internal assessment found a potential breach in the sterile barrier.
Product
Feeding Tube Metric, disposable, sterile, 100 eaches per sales unit. Labeled as: xray CH05/40CM and xray CH08/40CM Product Usage: Duodenal and Stomach Gastroenterology Tubes are sterile disposable devices which may be inserted through the nose or mouth via the esophagus into…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1019-2019·2019-03-27
AAP Implantate Lambotte Chisel Recalled for Potential Breakage at Welded Parts
AAP Implantate AG is recalling 25 units of the 20 mm Lambotte chisel due to a potential risk of breaking at the welded piece parts of the chisel body and knocking plate.
Product
aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1021-2019·2019-03-27
Advanced Pharma Recalls Glycopyrrolate Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 2,580 syringes of Glycopyrrolate Injectable Solution nationwide due to a lack of assurance of sterility.
Product
Glycopyrrolate Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe, NDC: 42852-828-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·19V243000·2019-03-27
Osco Recalls Emergency Vehicles With Faulty Brake Light Wiring
Osco Tank & Truck Sales is recalling 16,342 emergency vehicles built on 2012 Kenworth T440 and 2018 Peterbilt 348 chassis because brake lights may illuminate without the pedal being pressed.
Product
KENWORTH — KENWORTH, PETERBILT T440, 348
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V244000·2019-03-27
Toyota Recalls 2019 Models Due to Illegible Load Capacity Labels
Toyota is recalling specific 2019 models because the load capacity label text may become illegible, potentially leading to vehicle overload and increased crash risk.
Product
TOYOTA — TOYOTA CAMRY, AVALON, PRIUS, RAV4
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V241000·2019-03-27
Volkswagen Recalls 2019 Tiguan LWB for Inaccurate Tire Information Label
Volkswagen is recalling 2019 Tiguan LWB vehicles because the tire information label contains inaccurate dimension and pressure specifications, which may increase crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN TIGUAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1037-2019·2019-03-27
ConvaTec Recalls Nelaton Urinary Catheters Due to Sterile Barrier Breach Risk
ConvaTec is recalling Nelaton Urinary Catheters because an internal assessment found a potential breach in the sterile barrier, which could compromise the device's sterility.
Product
Nelaton Urinary Catheter, disposable, sterile, 100 eaches per sales unit. Labeled as: CH16/40CM and CH14/40CM Product Usage: Urinary Catheters are sterile disposable devices intended to provide an intermittent pathway for drainage of fluids from the bladder. They are…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19091·2019-03-27
Cambridge Elevating Recalls Home Elevators Due to Fall Hazard
Cambridge Elevating is recalling approximately 680 home elevators because the landing door can unlock without the elevator present, posing a fall hazard.
Product
Home elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1027-2019·2019-03-27
CP Medical Recalls Sterile Surgical Sutures Due to Potential Sterility Compromise
CP Medical Inc is recalling Plain and Chromic Gut Absorbable Surgical Sutures because routine endotoxin testing showed an out-of-limit result, potentially compromising sterility.
Product
Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic procedures, but not for use in cardiovascular and neural…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1020-2019·2019-03-27
FDA Recalls 850 Units of Covidien Force TriVerse Electrosurgical Devices
The FDA is recalling 850 units of the Covidien Force TriVerse electrosurgical device due to potential sterile packaging compromise.
Product
Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such as general, urologic, thoracic, plastic and reconstructive, gynecologic) and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1015-2019·2019-03-27
Siemens Dimension Vista 1500 Analyzer Recall Due to Water Module Contamination
Siemens is recalling 5,373 Dimension Vista 1500 analyzers because specific water purification modules may cause falsely elevated triglyceride results.
Product
Dimension Vista 1500, Analyzer, chemistry Model no. 10444801
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1033-2019·2019-03-27
ACell Recalls Gentrix Surgical Matrix Thick Due to Tensile Strength Failure
ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick because a sample failed to meet tensile strength specifications.
Product
Gentrix Surgical Matrix Thick, 20 x 30cm, Catalog Number PSMT2030, Lot 013948 - Product Usage: Gentrix Surgical Matrix Thick is intended for implantation to reinforce soft tissue where weakness exists in patients requiring gastroenterological or plastic and reconstructive…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1014-2019·2019-03-27
Siemens Dimension Vista 500 Analyzer Recall for Water Module Contamination
Siemens is recalling 5,373 Dimension Vista 500 analyzers because specific Millipore water purification modules may cause falsely elevated triglyceride results.
Product
Dimension Vista 500, Analyzer, chemistry Model no. 10284473
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1011-2019·2019-03-27
Akorn Recalls Hydrocortisone and Acetic Acid Otic Solution Due to Low Potency
Akorn Inc is recalling Hydrocortisone and Acetic Acid Otic Solution because routine stability testing revealed the drug was sub-potent.
Product
Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL per dropper bottle, Rx only, Hi-Tech Pharmacal Co, Inc., Amityville, NY 11701. NDC: 50383-901-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1038-2019·2019-03-27
ConvaTec Recalls FilterFlow Suction Handles Due to Sterile Barrier Breach Risk
ConvaTec is recalling 124,000 FilterFlow Suction Handles because an internal assessment found a potential breach in the sterile barrier.
Product
FilterFlow Suction Handle CH24, 20 eaches per sales unit. Product Usage: Filter Flow is designed for orthopedic surgery and combines suctioning function with filtering. The device is intended for orthopedic surgical procedures to remove and collect debris and bone fragments…
Category
Medical Device
Distribution
Distributed nationwide