State

Kansas product recalls

20,371 recalls have nationwide distribution and so reach Kansas. 0 additional recalls listed Kansas specifically in their distribution scope.

About recalls in Kansas

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Kansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14201–14225 of 20371

HighFDA (Devices)·Z-1118-2023·2023-02-22
Surgical Convenience Kits Recalled Due to Compromised Sterility of External Wrapping
Medline Industries is recalling 630 surgical convenience kits because the perforated bag design fails to maintain sterility of the outer wrapping, though internal contents remain sterile.
Product
Surgical convenience kits labeled as: a) MEDLINE GENERAL UTILITY, Reorder Number DYNDA2524 b) CENTURION MEDICAL PRODUCTS DIALYSIS ON/OFF BUNDLE, Reorder Number DT22705A c) CENTURION MEDICAL PRODUCTS ULTRASOUND PIV BUNDLE, Reorder Number IV8635D d) CENTURION MEDICAL PROD
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0279-2023·2023-02-22
Injectable Cefazolin-Heparin Syringes Recalled Nationwide for Lack of Sterility Assurance
Sentara Infusion Services is recalling compounded Cefazolin/Heparin injectable syringes due to lack of sterility assurance. Eight syringes with a December 2022 beyond-use date are affected.
Product
CEFAZOLIN 5mg/mL/HEPARIN 100unit/ml 1.5ML SYR, antibiotic, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0306-2023·2023-02-22
Metronidazole injectable antibiotic recalled due to sterility concerns
Sentara Infusion Services is recalling 30 bags of Metronidazole 500mg injectable antibiotic distributed nationwide due to lack of sterility assurance. Patients using the product should contact their healthcare provider.
Product
METRONIDAZOLE 500MG 100ML, antibiotic, Rx Only, use with a home pump or no pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0321-2023·2023-02-22
FDA Recalls TPN Nutrition Bags Due to Sterility Assurance Failure
Sentara Infusion Services recalls 24 bags of TPN (Total Parenteral Nutrition) distributed nationwide due to lack of sterility assurance. The recall affects prescription intravenous nutrition products.
Product
TPN (a) 95GM/AA, 385/DEX, 50GM/LIP 1800ML, (b)TPN AA:100GM DEX:250GM LIP:50GM 2400ML, (c) TPN: AA 80GM ; DEX 320GM ; LIP 50GM IN 2300 ml, Rx only, use with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1111-2023·2023-02-22
Medline surgical convenience kits recalled for inadequate exterior sterility
Medline is recalling surgical convenience kits because the perforated bag does not maintain sterility of the kit's exterior wrapping. Only the contents inside the wrapping are sterile.
Product
Surgical convenience kits labeled as: MEDLINE PERF. ASSOC. CUT DOWN TRAY, Reorder Number BM17BAD
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1133-2023·2023-02-22
iTotal Identity Impactor Handle surgical screws may loosen during procedures
Conformis Inc. is recalling the iTotal Identity Impactor Handle due to potential loose screws that could fall into patients during surgical procedures. Approximately 70 units from lot D221301 were distributed across multiple U.S. states.
Product
iTotal Identity Impactor Handle, Model No. 1080-212/ED-07827 REV AE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0297-2023·2023-02-22
Antibiotic Injectable Recalled for Lack of Sterility Assurance
Sentara Infusion Services is recalling an antibiotic injectable medication due to lack of sterility assurance. Seven bags were dispensed to patients nationwide with a Beyond Use Date of December 2022.
Product
IMIPENEM/CILASTATIN 2000MG IN NS 400ML, antibiotic, Rx Only, use with a Curlin Pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320, NDC# 63323-0322-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0295-2023·2023-02-22
Hydrocortisone Sterile Injection Syringes Recalled for Lack of Sterility Assurance
Sentara Infusion Services is recalling Hydrocortisone sterile injection syringes nationwide due to lack of sterility assurance. Patients who received affected syringes should contact their physician immediately.
Product
HYDROCORTISONE 9a) 2MG IN NS 0.2ML SYRINGE, 9MG IN NS 2ML SYRINGE, steroid, Rx Only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320, NDC# 00009-0011-04
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0274-2023·2023-02-22
Ampicillin Injectable Solution Recalled Due to Lack of Sterility Assurance
Sentara Infusion Services is recalling Ampicillin 12GM in NS 600M injectable solution due to lack of sterility assurance. The affected product was dispensed nationwide; patients should contact their healthcare provider.
Product
AMPICILLIN 12GM IN NS 600M, used with a Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1115-2023·2023-02-22
Surgical Tracheostomy Kit Recalled Due to Perforated Outer Wrapping Compromising Sterility
Medline Industries has recalled 120 units of Centurion Medical Products Tracheostomy Tray due to a perforated outer bag that prevents the exterior from remaining sterile, though the kit contents remain sterile.
Product
Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS TRACHEOSTOMY TRAY, Reorder Number TC7470
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0326-2023·2023-02-22
FDA Recalls Humatrix Microclysmic Gel for Manufacturing Practice Violations
Consolidated Chemical, Inc. is recalling 3186 bottles of Humatrix Microclysmic Gel nationwide due to deviations from proper manufacturing practices.
Product
Humatrix Microclysmic Gel, 8 oz per bottle, Care-Tech Laboratories, Inc., Saint Louis, Missouri 63139.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1131-2023·2023-02-22
HydroPICC Catheters Recalled for Incorrect Expiration Date Labeling
Access Vascular, Inc is recalling HydroPICC 4Fr Single Lumen catheters (Model 80001001) due to incorrect expiration date labeling. The devices expire earlier than the labeled date.
Product
HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1127-2023·2023-02-22
Surgical Circumcision Kits Recalled Due to Non-Sterile Outer Wrapping
MEDLINE INDUSTRIES is recalling CENTURION MEDICAL PRODUCTS Circumcision Tray kits (Lot 22HMH649) because the outer packaging is non-sterile, though the surgical contents inside remain sterile.
Product
Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS CIRCUMCISION TRAY, Reorder Number CIT3345
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0325-2023·2023-02-22
FDA recalls Techni-Care Chloroxylenol antiseptic due to manufacturing deviations
Consolidated Chemical is recalling Techni-Care Chloroxylenol 3% in 4 oz and 8 oz bottles nationwide due to manufacturing practice violations. No illnesses have been reported.
Product
Techni-Care Chloroxylenold 3%, [4 fl oz /118 mL or 8 fl oz/236 mL] per bottle, Care-Tech Laboratories, Inc., Saint Louis, Missouri 63139. NDC 4 oz bottle: 46706-222-01; NDC 8 oz: 46706-222-02
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·23126·2023-02-16
Paradise Grills First Generation Outdoor Kitchens Recalled for Fire and Burn Hazards
About 18,000 Paradise Grills First Generation Outdoor Kitchens are recalled because liquid propane gas can accumulate in the closed lid and cabinets, causing an explosion and severe burns when the grill is relit. Two reports of explosions causing severe burns have been received.
Product
Paradise Grills First Generation Outdoor Kitchens
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23120·2023-02-16
Wicked Lights ScanPro Night Hunting Headlamps Recalled for Burn Hazard
AllPredatorCalls.com is recalling approximately 12,000 Wicked Lights ScanPro night hunting headlamps because a wire short can cause the wire to heat up and melt, posing a burn hazard. The company has received 14 reports of wire heating and melting, including two burn injuries.
Product
Wicked Lights ScanPro Night Hunting Headlamps
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23127·2023-02-16
Kids Preferred Disney Character Figurines Recalled for Choking Hazard
Kids Preferred is recalling soft vinyl Disney character figurines because the arms or legs can detach, posing a choking hazard to children. About 16,140 units were sold nationwide through retailers including BuyBuy Baby and Amazon from May through December 2022.
Product
My First Mickey Mouse, Minnie Mouse, Buzz Lightyear, and Stitch Figurines
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23125·2023-02-16
KLIM Backcountry Probes A300 Recalled Due to Failure Risk
KLIM Backcountry Probes A300 can fail to operate when deployed to locate avalanche victims, posing a risk of severe injury or death. Consumers should stop using the product immediately and contact KLIM for a full refund.
Product
KLIM Backcountry Probes A300
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23123·2023-02-16
Children's Nightgowns Recalled for Flammability Standard Violation
Betsy & Lace children's nightgowns fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 90,550 units sold online from March 2018 through September 2022.
Product
Children's nightgowns
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23121·2023-02-16
Children's Nightgowns Recalled for Flammability Standard Violation
The Oaks Apparel Company is recalling about 320 children's nightgowns that fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop using them immediately.
Product
Children's nightgowns
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23122·2023-02-16
Hatley USA Children's Pajamas and Headbands Recalled
Hatley USA is recalling about 7,640 children's pajamas and about 300 headbands. The pajamas fail to meet federal flammability standards and pose a burn hazard; the headbands contain excess lead that is toxic if ingested.
Product
Children's pajamas and headbands
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23727·2023-02-16
Linus Bike Recalls Electric Bicycles Due to Crash Hazard
Linus Bike is recalling about 430 electric bicycles (Cesta 500 and Ero 500 models) because the front fork can crack, posing a crash hazard. No injuries have been reported.
Product
Electric bicycles
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1056-2023·2023-02-15
GE Nuclear Medicine Imaging Systems detector fall hazard
GE Nuclear Medicine 600/800 series imaging systems may have faulty detectors that could fall, causing serious injury. Mitigation measures may not be properly implemented on 34 units distributed worldwide.
Product
GE Nuclear Medicine 600/800 series systems, specifically: a) OPTIMA O640 X 3/8 inch NR, b) DISCOVERY O640 X 3/8 inch, c) NM OPTIMA O640 X 3/8 inch, d) O640 NM Gantry 3/8 inch, e) O640 NM GANTRY FINAL ASSY, f) OPTIMA O640 X 3/8 inch; Emission Computed Tomography System
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1058-2023·2023-02-15
GE Nuclear Medicine 600/800 Systems Recalled for Detector Fall Risk
GE Medical Systems is recalling 380 GE Nuclear Medicine 600/800 series diagnostic imaging systems worldwide due to potential failure in detector mitigation that could allow the detector to fall, risking life-threatening injury.
Product
GE Nuclear Medicine 600/800 series systems, specifically: a) 850, b) 850 / Dismount, c) 850 3/8 inch NM Gantry, d) 860 / Dismount, e) 860 3/8 inch NM Gantry, f) 860 5/8 inch NM Gantry, g) 860 BJ, h) NM 830 3/8 inch BJ, i) NM/CT 850 3/8 inch BJ, j) NM/CT 850 3/8 inch ROW,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1057-2023·2023-02-15
GE Nuclear Medicine Systems Recall Due to Potential Detector Fall Hazard
GE is recalling 86 Nuclear Medicine 600/800 series systems worldwide due to a potential failure in a safety mitigation. If not correctly implemented, the detector can fall and cause life-threatening injury.
Product
GE Nuclear Medicine 600/800 series systems, specifically: a) 870 CZT O540+ Gantry 7.25mm, b) D670 CZT Gantry 7.25mm, c) DISCOV NM/CT 870 CZT, d) Discovery NMCT 670 CZT O540+, e) NM/CT 870 CZT CYBER DEFENCE, f) NM/CT 870 CZT O540, g) NM/CT 870 CZT WSO, h) NM/CT 870 CZT, i
Category
Medical Device
Distribution
Distributed nationwide