State

Kansas product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50826–50850 of 79649

HighFDA (Drugs)·D-1484-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Tablets
Amerisource Health Services is recalling 867 cartons of 20 mg amphetamine tablets due to unit dose blister cavities containing more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 20 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2081-2016·2016-09-14
Lysander's Bourbon Flavor Rub Recalled for Undeclared Allergens
Geneva Foods is recalling Lysander's All Natural Bourbon Flavor Rub because it contains undeclared soy, wheat, and sulfites.
Product
Lysander's All Natural Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g), foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2066-2016·2016-09-14
Nature Made Adult Gummies Multi Recalled for Possible Salmonella Contamination
Pharmavite is recalling specific lots of Nature Made adult gummies Multi due to possible Salmonella contamination. Consumers should check lot numbers and expiration dates.
Product
Nature Made(R) adult gummies Multi, 150 count, UPC 0-31604-04172-4
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2071-2016·2016-09-14
Nature Made Super B-Complex Recalled for Possible Bacterial Contamination
Pharmavite is recalling Nature Made Super B-Complex vitamins due to possible Staphylococcus aureus and Salmonella contamination in specific lots.
Product
Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 460 count, UPC 0-31604-02728-5
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2072-2016·2016-09-14
Nature Made Super B-Complex Recalled for Possible Bacterial Contamination
Pharmavite is recalling Nature Made Super B-Complex supplements due to possible Staphylococcus aureus and Salmonella contamination in specific lots.
Product
Nature Made (R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 360 count, UPC 0-31604-02729-2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2765-2016·2016-09-14
Hologic Recalls SureSight Obturator Introducer Systems Due to Tip Breakage
Hologic is recalling 1,440 SureSight Obturator Introducer Localization Systems because the tip may break at the glue joint.
Product
SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI. ILS-0914-20-OB (9G Introducer Localization Set (OB Model) for ATEC0914-20MR Handpiece)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2737-2016·2016-09-14
Philips BrightView XCT Upgrade Recalled for Potential Patient Contact
Philips is recalling three BrightView XCT Upgrade units due to a software defect that may cause the detector to contact patients during specific scans.
Product
BrightView XCT Upgrade Model 882454
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2729-2016·2016-09-14
Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm
Hospira Inc. is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.
Product
Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2738-2016·2016-09-14
Terumo Recalls Pinnacle Introducer Sheaths Due to Valve Leakage
Terumo Medical Corporation is recalling Pinnacle Introducer Sheaths due to a manufacturing issue causing valve leakage, which poses a risk of incremental blood loss.
Product
PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Introducer Sheath
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2762-2016·2016-09-14
Riverpoint Medical Recalls Webglo Polypropylene Surgical Sutures Due to Seal Issues
Riverpoint Medical is recalling specific lots of Webglo polypropylene surgical sutures because the seals may open during distribution or packaging.
Product
Polypropylene Surgical Sutures, brand Webglo, for vet use. Product is sterile. Part number: GP8665 Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2763-2016·2016-09-14
Blackrock NeuroPort Biopotential Signal Processing System Recall for Labeling Error
Blackrock Microsystems is recalling 81 Neural Signal Amplifiers because the device and patient cable are incorrectly labeled as Type CF Applied Parts.
Product
Neural Signal Amplifier. Part Numbers: 4208, 5703, 5749, 5748, 5747. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes. Biopotential signals include…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2074-2016·2016-09-14
Nature Made Hair Skin Nails Gummies Recalled for Microbial Count
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Product
Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC 0-31604-04132-8-1
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2764-2016·2016-09-14
Blackrock NeuroPort Patient Cables Recalled for Incorrect Labeling
Blackrock Microsystems is voluntarily recalling 120 Patient Cables because they are incorrectly labeled as Type CF Applied Parts.
Product
Patient Cable. Part Numbers: 4460, 6735. Sterile within Chipboard Boxes within corrugated cartons. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1491-2016·2016-09-14
Zydus Recalls Bromocriptine Mesylate Capsules Due to Stability Test Failures
Zydus Pharmaceuticals is recalling 14,808 bottles of Bromocriptine Mesylate 5 mg capsules because stability samples failed impurity tests.
Product
BROMOCRIPTINE MESYLATE — BROMOCRIPTINE MESYLATE (BROMOCRIPTINE MESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2742-2016·2016-09-14
Siemens ADVIA Centaur PSA Assay Recall for Clinical Interpretation Clarification
Siemens Healthcare Diagnostics is recalling ADVIA Centaur PSA Assay kits to emphasize that PSA values must be interpreted according to current clinical guidelines for biochemical recurrence.
Product
ADVIA Centaur¿ PSA Assay; Cat No. 06574155/SMN 10310292 (100 test)/02676506/SMN 10310293 (500 test)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2073-2016·2016-09-14
Nature Made Hair Skin Nails Gummies Recalled for Microbial Count
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Product
Nature Made(R) adult gummies Hair.Skin.Nails, 90 count, UPC 0-31604-04016-1
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2747-2016·2016-09-14
Mentor Breast Tissue Expanders Recalled Due to Product Mix-Up
Mentor Texas, LP. is recalling 65 units of MENTOR CPX4 breast tissue expanders because a 350cc unit was found in a carton intended for 450cc units.
Product
MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1481-2016·2016-09-14
Amerisource Recalls Mispackaged Dextroamphetamine and Amphetamine Tablets
Amerisource Health Services is recalling 221 cartons of mixed amphetamine tablets due to unit dose mispackaging, where blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 5 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1494-2016·2016-09-14
Teva Recalls Argatroban Injection Due to Manufacturing Deviations
Teva North America is voluntarily recalling 1,299 bags of Argatroban Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL) , Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-0020-31 (Single Use Bag), NDC # 0703-0020-32 (5 Single Use Bags in One Carton).
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2743-2016·2016-09-14
Integra Recalls Achillon Suture System Due to Sterility Concerns
Integra LifeSciences is recalling the Achillon Suture System because internal studies suggest the secondary package seal may not maintain intended sterility.
Product
Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The Achillon Suture System is a single use, sterile device used to treat acute Achilles tendon ruptures. The Achillon Suture System is a mini-invasive procedure indicated to teat acute Achilles tendon…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2748-2016·2016-09-14
Mentor CPX4 Breast Tissue Expanders Recalled for Product Mix-Up
Mentor Texas, LP. is recalling 70 units of CPX4 breast tissue expanders because a 350cc product was found in a carton labeled for the 450cc version.
Product
MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2077-2016·2016-09-14
Nature Made Vitamin D Tablets Recalled for Yeast and Mold
Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.
Product
Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2075-2016·2016-09-14
Nature Made Vitamin D tablets recalled for yeast and mold
Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.
Product
Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2076-2016·2016-09-14
Nature Made Vitamin D Tablets Recalled for Potential Yeast and Mold
Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.
Product
Nature Made(R) D3 1000IU, 300 count, UPC 0-31604-02683-7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2759-2016·2016-09-14
Teleflex Horizon Manual-Load Ligating Clip Applier Recalled for Incorrect Etching
Teleflex Medical is recalling 49 units of Horizon Manual-Load Ligating Clip Appliers due to incorrect etching on the device.
Product
WECK¿ Horizon" Manual-Load Ligating Clip Applier, For Medium-Large Size Horizon Ligation Clips Curved Jaw, 11 (28cm), Rx Only, REF 337111, Product Usage: Weck Closure Systems applier has been designed and calibrated for use with specific Horizon, Hemoclip Plus Hemoclip…
Category
Medical Device
Distribution
Distributed nationwide