State

Kansas product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48426–48450 of 79646

ModerateFDA (Devices)·Z-1082-2017·2017-02-01
Atrium Medical Recalls Ocean Blood Recovery Drains Due to Sterility Issues
Atrium Medical is recalling Ocean Blood Recovery Drains because the outer packaging is not sterile. The recall affects units worldwide with expiration dates prior to October 2019.
Product
Atrium Medical Ocean Blood Recovery Drains as follows: 2050-000 Ocean Blood Recovery drain with in-line connector and suction control stopcock 2050-300 Ocean Blood Recovery drain with suction control stopcock, no in-line connector 2052-000 Ocean Double Blood Recovery drain…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0437-2017·2017-02-01
Roxane Recalls Furosemide Tablets Due to Unusually Thick Tablet Report
Roxane Laboratories is recalling 6,493 bottles of Furosemide 20 mg tablets because a complaint reported an unusually thick tablet.
Product
FUROSEMIDE — FUROSEMIDE (FUROSEMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0441-2017·2017-02-01
Mylan Recalls Temozolomide Capsules Due to Broken Capsules and Loose Powder
Mylan LLC is recalling specific lots of Temozolomide Capsules, 100 mg, because customer complaints reported broken or crushed capsules resulting in loose powder in the bottles.
Product
Temozolomide Capsules, 100 mg, packaged in a) 5-count bottles (NDC 0378-5262-98), b) 14-count bottles (NDC 0378-5262-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1078-2017·2017-02-01
Sekisui Diagnostics Ammonia L3K Assay Recalled for Performance Issues
Sekisui Diagnostics is recalling specific lots of the Ammonia L3K Assay because atypical optical density decreases may impact performance at the high end of the linear range.
Product
Sekisui Diagnostics Ammonia L3K¿ Assay; Catalog Number: 293-80-91 and 293-10 For the IN VITRO quantitative measurement of ammonia concentration in plasma
Category
Medical Device
Distribution
12 states
ModerateFDA (Food)·F-1358-2017·2017-02-01
Berner Food & Beverage Recalls Four Cheese Alfredo Pasta Sauce
Berner Food & Beverage is recalling 850 cases of Four Cheese Alfredo Pasta Sauce due to contamination with spoilage bacteria.
Product
Four Cheese Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NET 425g; Glass jar, metal lid; UPC 70038627838, 36800334793 or 041498198084
Category
Food
Distribution
7 states
ModerateFDA (Food)·F-1360-2017·2017-02-01
Berner Food Recalls Our Family Alfredo Pasta Sauce Due to Bacteria
Berner Food & Beverage, LLC is recalling Our Family Alfredo Pasta Sauce contaminated with spoilage bacteria. Consumers should discard the product.
Product
Our Family Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NET 425g; Glass jar, metal lid; UPC 70253266867
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-1100-2017·2017-02-01
PerkinElmer AutoDELFIA Plate Processor Recalled for Potential Loading Failures
PerkinElmer is recalling AutoDELFIA Plate Processors with Version 3.0 software due to potential plate loading failures that could affect clinical assay results.
Product
AutoDELFIA¿ Plate Processor , Fluorometer, for clinical use Product Number: 1235-5110 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the proven…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0443-2017·2017-02-01
Mylan Recalls Temozolomide Capsules Due to Broken Capsules and Loose Powder
Mylan LLC is recalling Temozolomide Capsules, 180 mg, due to customer complaints of broken or crushed capsules resulting in loose powder in the bottles.
Product
Temozolomide Capsules, 180 mg, packaged in a) 5-count bottles (NDC 0378-5264-98), b) 14-count bottles (NDC 0378-5264-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1086-2017·2017-02-01
Atrium Medical Recalls Oasis Blood Recovery Drains Due to Sterility Issues
Atrium Medical is recalling Oasis Blood Recovery Drains because the outer packaging is not sterile. The recall covers units with expiration dates prior to October 2019.
Product
Atrium Medical Oasis Blood Recovery Drains as follows: 3650-100 Oasis Blood Recovery drain with in-line connector 3652-100 Oasis Double Blood Recovery drain with in-line connectors - 2 patient lines connected by one Y connector Product Usage: To evacuate air and/or fluid…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1087-2017·2017-02-01
Atrium Medical 400 Series Express Drains Recalled for Non-Sterile Packaging
Atrium Medical is recalling 400 Series Express Drains because the outer packaging is not sterile. The recall affects approximately 1.4 million cases distributed worldwide.
Product
Atrium Medical 400 Series Express Drains as follows: 4000-100N Express single collection drain with in-line connector 4000-100P Express PreFilled Chest Drain 4020-100N Express dual chamber drain with in-line connectors ( 2 Patient Tubes) 4050-100N Express Blood Recovery…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0446-2017·2017-02-01
Sun Pharmaceutical Recalls BuPROPion Hydrochloride Tablets for Dissolution Failures
Sun Pharmaceutical Industries is recalling 11,618 bottles of buPROPion Hydrochloride Extended-release Tablets due to failed dissolution specifications and stability issues.
Product
buPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, 60 count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0442-2017·2017-02-01
Mylan Recalls Temozolomide Capsules Due to Broken Capsules and Loose Powder
Mylan LLC is recalling Temozolomide Capsules, 140 mg, due to customer complaints of broken or crushed capsules resulting in loose powder in the bottles.
Product
Temozolomide Capsules, 140 mg, packaged in a) 5-count bottles (NDC 0378-5263-98), b) 14-count bottles (NDC 0378-5263-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1084-2017·2017-02-01
Atrium Medical Oasis Pediatric Drain Recalled for Non-Sterile Packaging
Atrium Medical is recalling Oasis Pediatric Drains because the outer packaging is not sterile. The recall covers 964,463 US cases and 521,975 international cases.
Product
Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis Infant/Pediatric drain with in-line connector, ¿ in. tubing, Sims and Pedi connector in bag on back of drain 3612-400 Oasis Infant/Pediatric drain with no in-line connector, ¿ in. tubing, Sims and Pedi connector…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1088-2017·2017-02-01
Atrium Medical Express Mini 500 Dry Seal Drain Recall
Atrium Medical is recalling Express Mini 500 dry seal drains because the outer packaging is not sterile.
Product
Atrium Medical 16400 Express Mini 500 dry seal drain Product Usage: To evacuate air and/or fluid from the chest cavity or mediastinum. To help re-establish lung expansion and restore breathing dynamics. To facilitate postoperative collection and reinfusion of autologous…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1102-2017·2017-02-01
PerkinElmer AutoDELFIA System Recalled for Potential Plate Loading Failures
PerkinElmer is recalling AutoDELFIA systems with V3.0 software due to potential plate loading failures that could affect clinical assay results.
Product
DELFIA¿ PC with V3.0 Software, Fluorometer, for clinical use Product Number: 1235-8100 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the proven…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0448-2017·2017-02-01
Roxane Recalls Azelastine Nasal Spray Due to Defective Delivery System
Roxane Laboratories is recalling 74,108 bottles of Azelastine Hydrochloride Nasal Spray because the delivery system failed droplet size testing.
Product
Azelastine Hydrochloride Nasal Solution (Nasal Spray), 0.1% (137 mcg per spray), packaged in 30 mL bottles, Rx only, Distributed by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-0293-99
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1101-2017·2017-02-01
PerkinElmer AutoDELFIA System Recalled for Potential Plate Loading Failures
PerkinElmer is recalling AutoDELFIA systems with Version 3.0 software due to potential plate loading failures that could affect clinical assay results.
Product
Program Update Package AutoDELFIA¿ 3.0, Fluorometer, for clinical use Product Number: 1235-8110 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0438-2017·2017-02-01
Qualitest Recalls Dexamethasone Elixir Due to Failed Impurity Specifications
Vintage Pharmaceuticals is recalling 2,568 bottles of Dexamethasone Elixir because the product failed impurity and degradation specifications.
Product
DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL, NDC 0603-1147-56
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1075-2017·2017-02-01
Pentax Rigid Laryngostroboscopes Field Correction for Instructions for Use
Pentax of America is revising the Instructions for Use for Rigid Laryngostroboscopes Models 9106 and 9108.
Product
Rigid Laryngostroboscopes The Rigid Laryngostroboscopes, Models 9106 and 9108 are intended to observe glottic action with the use of a stroboscopic light source. The instrument is inserted per-orally when indications consistent with the need for observation are observed.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0439-2017·2017-02-01
Actavis Recalls Albuterol Sulfate Inhalation Solution Due to Impurities
Actavis Inc is recalling specific lots of Albuterol Sulfate Inhalation Solution because the product failed impurity specifications for a known degradant.
Product
Albuterol Sulfate Inhalation Solution, USP, 0.021% (0.63 mg / 3 mL), 3mL Vials, Rx only, Mfd. for Watson Laboratories Inc., Corona, CA 92880 USA, Mfd. by Cipla Ltd. Verna, Goa India, NDC 0591-3467-53
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·17730·2017-01-31
Simpli Home Recalls Chests of Drawers Due to Tip-Over Hazard
Simpli Home is recalling about 240 chests of drawers because they can tip over and injure children if not anchored to the wall.
Product
Chest of drawers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·17078·2017-01-31
Bar Chairs Recalled Due to Fall Hazard from Detaching Legs
3i Corporation is recalling bar chairs sold at Lowe's because legs can detach from the center post, posing a fall hazard.
Product
Bar chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·17075·2017-01-31
Bolton Furniture Recalls 4-Drawer Dressers Due to Tip-Over Hazards
Bolton Furniture is recalling approximately 1,000 4-drawer dressers because they pose a serious tip-over and entrapment hazard to children if not anchored to the wall.
Product
Two Over Two 4-drawer dressers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17077·2017-01-31
Brown Jordan Recalls Swivel Patio Chairs Due to Fall Hazard
Brown Jordan Services is recalling La-Z-Boy swivel patio chairs sold at Sears.com because the base can break during normal use, posing a fall hazard.
Product
Swivel Patio Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17731·2017-01-31
South Shore Recalls 5-Drawer Chests Due to Tip-Over and Entrapment Hazards
South Shore is recalling 5-drawer chests that pose tip-over and entrapment hazards to children if not anchored to the wall.
Product
5-drawer chests
Category
Consumer Product
Distribution
Distributed nationwide