State

Kansas product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30776–30800 of 79543

HighFDA (Drugs)·D-1304-2020·2020-06-24
AvKARE Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity
AvKARE Inc. is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Product
Metformin Hydrochloride Extended-Release Tablets, USP 750 mg a) 90 count (NDC 42291-611-90) b) 180 count (NDC 42291-611-18) c) 500 count (NDC 42291-611-50) bottles, Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2371-2020·2020-06-24
Biosense Webster Recalls PENTARAY NAV High-Density Mapping Catheters
Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because they can become entrapped in the heart's valves during use.
Product
PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster PENTARAY NAV High-Density Mapping Catheter is indicated for multiple electrode electrophysiological mapping of cardiac structures in the heart, i.e.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2396-2020·2020-06-24
AngioDynamics PICC Kits Recalled Due to Defective Saline Flush Syringes
AngioDynamics is recalling certain PICC Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical.
Product
BioFlo Midline Convenience Kits - Product Usage: These introducers are used for the percutaneous introduction of diagnostic or therapeutic devices, such as catheters or pacing leads in the vasculature. Item Numbers H96560M0125711 H96560M0133541 H96560M0354721…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1325-2020·2020-06-24
Gaviscon Liquid Antacid Recalled for Missing Magnesium Safety Warning
Gaviscon Liquid Antacid Extra Strength is being recalled because the bottle label lacks a required magnesium safety warning. The recall covers single and twin-pack bottles distributed nationwide.
Product
GAVISCON — GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2364-2020·2020-06-24
Ortho-Clinical Diagnostics Recalls VITROS AMYL Slides Reagent for Imprecision
Ortho-Clinical Diagnostics is recalling VITROS AMYL Slides Reagent because multiple coatings show imprecision on control fluids. The product is used for in vitro diagnostic testing.
Product
VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/300 SLDS, Product Code 1202670, UDI # 10758750008513 - Product Usage: For in vitro diagnostic use only to quantitatively measure amylase activity in serum, plasma, and urine using VITROS 250/350/5, 1 FS/4600/XT 3400…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2398-2020·2020-06-24
AngioDynamics Recalls PICC Kits Containing Recalled BD Saline Flush Syringes
AngioDynamics is recalling BioFlo and Xcela PICC kits because they contain BD saline flush syringes that were previously recalled by BD Medical.
Product
BioFlo PICC and Xcela PICC Maximal Barrier Nursing Kits - Product Usage: are indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications and nutrients; the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1308-2020·2020-06-24
Hikma Recalls Irinotecan Hydrochloride Injection Due to Container Defect
Hikma Pharmaceuticals is recalling 82,426 vials of Irinotecan Hydrochloride Injection due to a crimp defect in the flip-cap.
Product
IRINOTECAN HYDROCHLORIDE — IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2369-2020·2020-06-24
Resource Optimization Recalls Regard SRHS Central Line Kits Due to Packaging Defects
Resource Optimization & Innovation LLC is recalling Regard SRHS Central Line Kits because holes in the packaging may compromise the sterile field.
Product
Regard SRHS Central Line Kit, Sterile, 20/case - Product Usage: The Saline Flush Syringes are intended to be used only for the flushing of indwelling of vascular access devices.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1309-2020·2020-06-24
Hikma Recalls Irinotecan Hydrochloride Vials Due to Container Defect
Hikma Pharmaceuticals is recalling 17,998 vials of Irinotecan Hydrochloride Injection due to a crimp defect in the flip-cap.
Product
IRINOTECAN HYDROCHLORIDE — IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1324-2020·2020-06-24
Gaviscon Extra Strength Liquid Antacid Recalled for Missing Magnesium Warning
GSK is recalling Gaviscon Extra Strength Liquid Antacid because the bottle label is missing a required magnesium safety warning.
Product
Gaviscon Extra Strength Liquid Antacid Extra Strength Cherry, 12 FL OZ. (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0574-41
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2365-2020·2020-06-24
Ortho-Clinical Diagnostics Recalls VITROS AMYL Slides Reagent for Imprecision
Ortho-Clinical Diagnostics is recalling VITROS AMYL Slides Reagent because multiple coatings show imprecision on control fluids compared to expected standards.
Product
VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/90 SLDS, Product Code 8112724, UDI # 10758750004393 - Product Usage: For in vitro diagnostic use only to quantitatively measure amylase activity in serum, plasma, and urine using VITROS 250/350/5, 1 FS/4600/XT 3400…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2395-2020·2020-06-24
AngioDynamics Recalls PICC Kits Containing Recalled BD Syringes
AngioDynamics is recalling certain PICC Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical.
Product
BioFlo Midline Catheter and BioFlo Maximal Barrier Kits - Product Usage: These introducers are used for the percutaneous introduction of diagnostic or therapeutic devices, such as catheters or pacing leads in the vasculature. Item Numbers H965460151 H965460161…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1323-2020·2020-06-24
Gaviscon Antacid Recalled for Missing Magnesium Safety Warning
Gaviscon Regular Strength Liquid Antacid is being recalled because the bottle label lacks the required magnesium safety warning.
Product
GAVISCON — GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2366-2020·2020-06-24
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Product Performance Verifier I
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Product Performance Verifier I units because multiple coatings of AMYL Slides show imprecision on control fluids.
Product
VITROS Chemistry Product Performance Verifier I, Product Code 8231474, UDI # 10758750004577 - Product Usage: For in vitro diagnostic use only to quantitatively measure amylase activity in serum, plasma, and urine using VITROS 250/350/5, 1 FS/4600/XT 3400 Chemistry Systems and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1310-2020·2020-06-24
EcoLips Sport Lip Balm Recalled for Excessive Avobenzone Concentration
Eco Lips Inc. is recalling 68,400 tubes of EcoLips Sport Lip Balm, SPF 30, because the avobenzone concentration exceeds FDA limits.
Product
EcoLips Sport Lip Balm, SPF 30, Avobenzone (5%), Octinoxate (10%), Octisalate (5%), Net Wt. 0.15 oz. (4.25g) tube, Eco Lips, Inc., Marion, IA 52302, UPC: 859623000030; 859623000177; 859623000573; Display UPC: 859623000092; 859623000108; 859623000139; 859623000146; 859623000184…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2367-2020·2020-06-24
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Product Performance Verifier II
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Product Performance Verifier II units because multiple coatings of AMYL Slides show imprecision on control fluids.
Product
VITROS Chemistry Product Performance Verifier II, Product Code 8067324, UDI # 10758750004317 - Product Usage: For in vitro diagnostic use only to quantitatively measure amylase activity in serum, plasma, and urine using VITROS 250/350/5, 1 FS/4600/XT 3400 Chemistry Systems and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1322-2020·2020-06-24
Gaviscon Antacid Recalled for Missing Magnesium Safety Warning
GSK is recalling Gaviscon Regular Strength Liquid Antacid bottles because the labels lack a required magnesium safety warning.
Product
GAVISCON — GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
LowNHTSA·20V372000·2020-06-24
Volkswagen Recalls Two 2018 Golf GTI Vehicles for VIN Label Mismatch
Volkswagen is recalling two 2018 Golf GTI vehicles because the VIN on the Federal Certification label may not match the actual vehicle VIN, potentially preventing owners from identifying safety recalls.
Product
VOLKSWAGEN — VOLKSWAGEN GOLF
Category
Vehicle
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1315-2020·2020-06-24
Aurobindo Recalls Olanzapine Tablets Due to Failed Impurity Specifications
Aurobindo Pharma USA Inc. is recalling Olanzapine Tablets, USP 7.5 mg, because the product failed impurity and degradation specifications.
Product
Olanzapine Tablets, USP 7.5 mg, 30-count bottle, Rx only, Manufactured for: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Aurolife Pharma LLC Dayton, NJ 08810, NDC 66993-682-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1314-2020·2020-06-24
Aurobindo Pharma Recalls Olanzapine Tablets Due to Impurity Failures
Aurobindo Pharma USA Inc. is recalling Olanzapine Tablets, USP 2.5 mg, because the product failed impurities and degradation specifications.
Product
Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx only, Manufactured for: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Aurolife Pharma LLC Dayton, NJ 08810, NDC 66993-680-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2370-2020·2020-06-24
Abbott Vascular Recalls Xience Sierra Stents Due to Incorrect Expiration Date
Abbott Vascular is recalling 13 units of Xience Sierra coronary stents because they bear an incorrect expiration date.
Product
Xience Sierra TM Everolimus Eluting Coronary Stent System, RX 3.5mm x 33mmStrength: 100 ¿g/cm¿, Nominal Everolimus Content: 209 ¿g; Lot number 903224A,
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V365000·2020-06-23
Ford Recalls 2020 Super-Duty Pickups for Transmission Defect
Ford is recalling 2020 F-250, F-350, and F-550 Super-Duty diesel pickups because a brittle transmission part may fracture, causing engine stalls or increased braking effort.
Product
FORD — FORD F-250 SD, F-550 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V367000·2020-06-23
Newell P50 Motor Coaches Recalled for Brake Pedal Obstruction Risk
Newell is recalling 2020-2021 P50 motor coaches because a decorative cover may become lodged under the brake pedal, potentially impacting the ability to stop.
Product
NEWELL — NEWELL P50
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V366000·2020-06-23
Ford Recalls 2020 Expedition and Lincoln Navigator for Headrest Weld Defect
Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because a driver's side second-row seat headrest bracket may be improperly welded, potentially failing to restrain occupants in a crash.
Product
FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V364000·2020-06-22
Mercedes-Benz Recalls 2020 Models for Turbocharger Oil Leak Fire Risk
Mercedes-Benz is recalling 2020 C300, E350, and GLC300 vehicles because improperly tightened turbocharger oil line screws may cause leaks that increase fire risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ E 350, C 300, GLC 300
Category
Vehicle
Distribution
Distributed nationwide