State

Kansas product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35051–35075 of 79559

ModerateFDA (Drugs)·D-1740-2019·2019-08-21
US Pharmaceuticals Recalls Wonder Freeze Pain Gel Due to Water Quality Issues
US Pharmaceuticals is recalling Wonder Freeze Pain Relieving Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
Wonder Freeze Pain Releiving Gel with ILEX, Menthol 5%, packaged in a) 3 OZ /85 g (UPC 0 99528 35903 5); b) 4 OZ / 113 g (UPC 0 99528 31504 8); c) 16 OZ / 454 g (UPC 0 99528 31516 1); Manufactured For: Wonder Laboratories, 115 S.C.T. Ct., White House TN. 37188.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1727-2019·2019-08-21
US Pharmaceuticals Recalls Children's Glycerin Suppositories for Water Quality Issues
US Pharmaceuticals is recalling 76 cases of Children Glycerin Suppositories due to out-of-specification results in the purified water used during manufacturing.
Product
Children Glycerin Suppositories Laxative for ages 2 to 5. Package Size 25-count.Distributed by Walgreen CO. 200 Wilmot Rd. Deerfield IL 60015. NDC#0363-0440-25,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1741-2019·2019-08-21
US Pharmaceuticals Recalls CRYO-273 Cold Pain Gel Due to Water Quality Issues
US Pharmaceuticals is recalling CRYO-273 Cold Pain Relieving Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
CRYO-273 Cold Pain Relieving Gel 128 FL. OZ. Distributed By: CRYO-273.com Tampa, FL 33629. UPC 8 15290 01550 2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1736-2019·2019-08-21
CVS Health Glycerin Suppositories Recalled for Water Quality Issues
US Pharmaceuticals is recalling CVS Health Glycerin Suppositories because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
CVS Health Glycerin Suppositories, 100- count box, Distributed by:Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895. UPC 0 50428 42738 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1729-2019·2019-08-21
US Pharmaceuticals Recalls Adult Glycerin Suppositories Due to Water Quality Issues
US Pharmaceuticals is recalling 196 cases of Adult Glycerin Suppositories because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
Adult Glycerin Suppositories, Package Size 50-count suppositories, Distributed By: Walgreen Co. 200 Wilmot Rd. Deerfield, IL 60015. NDC#0363-0441-50
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1731-2019·2019-08-21
US Pharmaceuticals Recalls Hydrocortisone Cream Due to Water Quality Issues
US Pharmaceuticals is recalling Maximum Strength Hydrocortisone Cream with Aloe due to out-of-specification results in the purified water used during manufacturing.
Product
MAXIMUM STRENGTH HYDROCORTISONE CREAM WITH ALOE — MAXIMUM STRENGTH HYDROCORTISONE CREAM WITH ALOE (HYDROCORTISONE CREAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1732-2019·2019-08-21
US Pharmaceuticals Recalls Hydrocortisone Cream Due to Water Quality Issues
US Pharmaceuticals is recalling specific lots of Maximum Strength Hydrocortisone Cream with Aloe because the purified water used in manufacturing failed quality tests.
Product
MAXIMUM STRENGTH HYDROCORTISONE CREAM WITH ALOE — MAXIMUM STRENGTH HYDROCORTISONE CREAM WITH ALOE (HYDROCORTISONE CREAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2283-2019·2019-08-21
Luminex ARIES HSV 1&2 Assay Recalled for Seal Defects
Luminex is recalling ARIES HSV 1&2 Assay kits because side cassette seals did not meet specifications, potentially affecting test sensitivity and stability.
Product
ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295
Category
Medical Device
Distribution
34 states
ModerateFDA (Drugs)·D-1728-2019·2019-08-21
US Pharmaceuticals Recalls Walgreens Glycerin Suppositories for Water Quality Issues
US Pharmaceuticals is recalling 98 cases of Walgreens Adult Glycerin Suppositories due to out-of-specification results in the purified water used during manufacturing.
Product
WALGREENS ADULT GLYCERIN — WALGREENS ADULT GLYCERIN (GLYCERIN SUPPOSITORY)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1737-2019·2019-08-21
US Pharmaceuticals Recalls CRYO-273 Cold Pain Gel Due to Water Quality Issues
US Pharmaceuticals is recalling CRYO-273 Cold Pain Relieving Gel Roll-On because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
CRYO-273 Cold Pain Relieving Gel Roll-On 3 FL. OZ. (89 mL) Distributed By: CRYO-273.com Tampa, FL 33629. UPC 8 15290 01529 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2286-2019·2019-08-21
Luminex ARIES Group A Strep Assay Recalled for Seal Defects
Luminex is recalling ARIES Group A Strep Assay kits because side cassette seals may not meet specifications, potentially affecting test sensitivity and stability.
Product
ARIES Group A Strep Assay , REF 50-10041, UDI # 00840487101469
Category
Medical Device
Distribution
34 states
ModerateFDA (Devices)·Z-2282-2019·2019-08-21
Luminex Aries Bordetella Assay Recalled for Partially Sealed Cassette Assemblies
Luminex Corporation is recalling Aries Bordetella Assay kits because partially sealed side cassette assemblies may reduce assay sensitivity or stability.
Product
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Category
Medical Device
Distribution
34 states
ModerateFDA (Drugs)·D-1726-2019·2019-08-21
US Pharmaceuticals Recalls CVS Therapeutic Menthol Gel Due to Water Quality Issues
US Pharmaceuticals is recalling CVS Therapeutic Menthol Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
CVS Therapeutic Menthol Gel, 8 FL OZ (227 g) Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895. UPC 0 50428 48136 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1735-2019·2019-08-21
US Pharmaceuticals Recalls Soothe&Cool Protect Moisture Guard Skin Protectant
US Pharmaceuticals is recalling 830 tubes of Soothe&Cool Protect Moisture Guard Skin Protectant due to out-of-specification results for microbial count or organic carbon in purified water.
Product
Soothe&Cool Protect Moisture Guard Skin Protectant, 3.5 oz. (99 g), tube, Manufactured for Medline industries, Inc., Mundelein, IL 60060. NDC 53329-303-22
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1724-2019·2019-08-21
CVS Health Glycerin Suppositories Recalled for Water Quality Issues
US Pharmaceuticals is recalling CVS Health Glycerin Suppositories due to out-of-specification results for microbial count or organic carbon in the purified water used during manufacturing.
Product
CVS Health Glycerin Suppositories, 50-count box, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895. UPC 0 50428 33106 4
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1821-2019·2019-08-21
Carbamazepine Extended-Release Tablets Recalled for Failed Dissolution Specifications
American Health Packaging is recalling Carbamazepine Extended-Release Tablets, 400 mg, because they failed to meet dissolution specifications.
Product
Carbamazepine, Extended-Release Tablets, USP, 400 mg, 30 Tablets (3 blister cards x 10 unit doses), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-562-21; NDC Unit Dose: 68084-562-11
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1738-2019·2019-08-21
US Pharmaceuticals Recalls Cool Hot Ice Analgesic Gel Due to Water Quality Issues
US Pharmaceuticals is recalling 246 cases of Cool Hot Ice Analgesic Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
Cool Hot Ice Analgesic Gel, 8 oz (227 g) Distributed by: Unipack Inc. Pittsburg, PA 15239, USA. UPC 7 51393 00608 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2288-2019·2019-08-21
Luminex ARIES Extraction Kit Recalled for Partially Sealed Cassette Assemblies
Luminex Corporation is recalling ARIES Extraction Kits because partially sealed side cassette assemblies may reduce assay sensitivity and stability.
Product
ARIES Extraction Kit; ARIES System; SYNCT , REF 50-10026, UDI # 00840487100073
Category
Medical Device
Distribution
34 states
ModerateFDA (Drugs)·D-1725-2019·2019-08-21
US Pharmaceuticals Recalls Intensive Healing Eczema Lotion for Water Quality Issues
US Pharmaceuticals is recalling Intensive Healing Eczema Lotion due to out-of-specification results for microbial count or organic carbon in the purified water used during manufacturing.
Product
INTENSIVE HEALING ECZEMA — INTENSIVE HEALING ECZEMA (HYDROCORTISONE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1743-2019·2019-08-21
Glenmark Recalls Clotrimazole and Betamethasone Cream Due to Temperature Abuse
Glenmark Pharmaceuticals is recalling 31,224 tubes of Clotrimazole and Betamethasone Dipropionate Cream due to complaints of a liquidy texture caused by temperature abuse.
Product
CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE — CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE (CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE)
Category
Drug
Distribution
Distributed nationwide
CriticalUSDA FSIS·085-2019·2019-08-20
Tip Top Poultry Recalls Fully Cooked Chicken Due to Listeria Risk
Tip Top Poultry is recalling approximately 135,810 pounds of fully cooked diced chicken products due to possible Listeria monocytogenes contamination.
Product
Silver Comet Foods, LLC (FKA Tip Top Poultry Inc.) distributed by Tip Top — Tip Top Poultry, Inc. Recalls Fully Cooked Poultry Products due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·19V609000·2019-08-20
Thor Motor Coach Recalls 2020 Motorhomes for Battery Cable Fire Risk
Thor Motor Coach is recalling 1,941 2020 motorhomes because loose battery cables may cause electrical arcing and increase the risk of a fire.
Product
THOR MOTOR COACH — THOR MOTOR COACH, THOR MAJESTIC, DAYBREAK, CHATEAU, OUTLAW
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19185·2019-08-20
SAMpark Recalls Children's Pajamas for Flammability Standard Violation
SAMpark is recalling about 185 children's pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Product
Children's pajamas
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19E055000·2019-08-20
Hale SmartFoam 6.5-12 Foam Pump Systems Recalled for Overheating Risk
Hale Products Inc. is recalling SmartFoam 6.5-12 foam pump systems with 12-volt power supplies because they can overheat and fail, rendering fire-fighting foam unavailable.
Product
EQUIPMENT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·19183·2019-08-20
Southwire Recalls Garvin Pop-Up Electrical Outlet Floor Box Kits Due to Fire Hazard
Southwire is recalling about 3,000 Garvin Pop-Up Electrical Outlet Floor Box Kits because the receptacles can overheat, posing a fire hazard. No injuries have been reported.
Product
Garvin Pop-Up Electrical Outlet Floor Box Kits
Category
Consumer Product
Distribution
Distributed nationwide