State

Kansas product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54326–54350 of 79655

HighFDA (Devices)·Z-0771-2016·2016-02-17
Accuray CyberKnife Robotic Recall for Potential Gun Box Mounting Bracket Failure
Accuray is recalling CyberKnife Robotic systems because the gun box mounting bracket may fail, allowing the gun box to fall and contact a patient.
Product
CyberKnife Robotic; Catalog/part number 032000 and 033000 Cosmetic cover package. Product Usage: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors, and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0761-2016·2016-02-17
Del Medical VS200 Radiographic Cassette Holder Recall for Falling Hazard
Del Medical is recalling VS200 radiographic cassette holders and wall stands because they can suddenly fall to the ground and contact patients.
Product
VS200 radiographic Cassette Holder or Wall Stand. For use in radiology department.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0763-2016·2016-02-17
GE Medical Systems Recalls Mavig Monitor Suspension System Due to Fall Risk
GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.
Product
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100, INNOVA 3131IQ, INNOVA 2121IQ, INNOVA 2100IQ, INNOVA 3100IQ, and INNOVA 4100IQ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2016·2016-02-17
Del Medical VS300 Radiographic Cassette Holder Recall for Falling Hazard
Del Medical, Inc. is recalling VS300 radiographic cassette holders and wall stands because the unit can suddenly fall to the bottom of its travel and contact a patient.
Product
VS300 radiographic Cassette Holder or Wall Stand. For use in radiology department.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0778-2016·2016-02-17
Zimmer Dental Implants Recalled for Missing Safety Information in Instructions
Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.
Product
IMPLANT,TM, MTX FULL 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMT4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0574-2016·2016-02-17
Bearded Brothers BOLD The Greek Energy Bars Recalled for Mold
Bearded Brothers LLC is recalling BOLD The Greek energy bars due to mold. The recall covers 150 cases distributed nationwide.
Product
Bearded Brothers BOLD The Greek Net Wt. 1.5 oz/43 g UPC: 8-50430-00414-2.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0783-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMTB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0773-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMM4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0781-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMTB10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0752-2016·2016-02-17
Toshiba INFX-8000V X-Ray System Recalled for Dose Meter Error
Toshiba is recalling four INFX-8000V Bi-Plane X-Ray Interventional Systems because a software error caused dose data to be lost during specific imaging procedures.
Product
INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0576-2016·2016-02-17
Bulletproof FATwater Lemon Bottles Recalled for Microbial Growth
Bulletproof Digital Inc is recalling FATwater Lemon bottles due to microbial growth detection. No pathogens were found.
Product
FATwater bottle, 16.9 fl. oz., Lemon flavor, UPC 6 09015 50475 8
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0656-2016·2016-02-17
Fagron Recalls SyrSpend SF Suspending Base Due to Yeast Contamination
Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product contains yeast. The recall covers 88 bottles distributed nationwide.
Product
SyrSpend SF, Suspending Base, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-9.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0772-2016·2016-02-17
Zimmer Dental Implants Recalled for Missing Instructions
Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.
Product
IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0774-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Product
IMPLANT,TM, MTX 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMM4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0795-2016·2016-02-17
PharmaCaribe PulmoSal 7% Sodium Chloride Inhalation Solution Recalled for Mislabeling
Pharmacaribe LLC is recalling PulmoSal 7% Sodium Chloride inhalation solution because vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+).
Product
PharmaCaribe PulmoSal 7% Sodium chloride, Inhalation Solution, 7% Sterile, Preservative -free, Non-pyrogenic, pH 7.4 For Inhalation Only Rx Product Usage: The contents of these vials are used in conjunction with a nebulizer for the induction of sputum production where…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0575-2016·2016-02-17
Bulletproof Recalls Berry FATwater Bottles Due to Microbial Growth
Bulletproof Digital Inc is recalling 12,583 bottles of Berry FATwater due to microbial growth detection. No pathogens were detected.
Product
FATwater bottle, 16.9 fl. oz., Berry flavor, UPC 6 09015 50477 2
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0573-2016·2016-02-17
Bearded Brothers BOLD Coconut Curry Energy Bars Recalled for Mold
Bearded Brothers LLC is recalling 128 cases of BOLD Coconut Curry energy bars due to mold. The product was distributed nationwide.
Product
Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g UPC: 8-50430-00513-5.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0794-2016·2016-02-17
Merge Healthcare Recalls RadSuite Picture Archive System for Measurement Errors
Merge Healthcare is recalling RadSuite picture archive systems because they may display incorrect Standardized Uptake Values (SUV). The recall covers 164 units distributed nationwide.
Product
RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344, 5.30.3, 5.30.4, 5.30.4 HF0418E, 5.30.5, 5.30.5 HF0404E, 5.30.5 HF0413E, 5.30.5 HF390E, 5.30.5 SB0368, 5.30.6, 5.30.6 HF0405E, 5.30.6 HF0406E, 5.30.7, 5.30.7…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0780-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX FULL 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMT4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0659-2016·2016-02-17
Sandoz Recalls Candesartan Cilexetil Tablets Due to Impurity Failures
Sandoz Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because the product failed impurities and degradation specifications at a 9-month stability timepoint.
Product
Candesartan Cilexetil Tablets, 16 mg, a) 30 count (NDC 00781-5938-31) and b) 90 count (NDC 00781-5938-92) bottles, Rx Only, Manufactured by Mylan Laboratories Limited Hyderabad 500 034, India for Sandoz Inc. Princeton, NJ 08540
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0776-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc is recalling specific dental implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMMB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0577-2016·2016-02-17
Bulletproof Recalls Tangerine FATwater Bottles Due to Microbial Growth
Bulletproof Digital Inc is recalling 5,748 bottles of Tangerine FATwater due to microbial growth detection. No pathogens were detected.
Product
FATwater bottle, 16.9 fl. oz., Tangerine flavor, UPC 6 41871 93693 9
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0775-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Instructions in Manual
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because critical safety information was missing from the instruction manual.
Product
IMPLANT,TM, MTX 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMMB10 Product Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or more…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0758-2016·2016-02-17
Spectranetics Recalls Expired 2.3mm Turbo-Power Laser Atherectomy Catheters
Spectranetics Corp. is recalling 8 units of 2.3mm Turbo-Power OTW Manual laser atherectomy catheters because they are past their expiration date.
Product
2.3mm Turbo-Power OTW, Manual, Model No 423-050 Product Usage The Turbo-Power System (Laser Atherectomy Catheter) is a laser atherectomy device designed for use with the CVX-300" Excimer Laser System. The Turbo-Power Laser Atherectomy Catheter is a sterile, single use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0779-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the latest instructions for use.
Product
IMPLANT,TM, MTX FULL 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMT4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace…
Category
Medical Device
Distribution
Distributed nationwide