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Kimberly-Clark Recalls
19 recalls on record · July 18, 2012 to April 14, 2021 · Drugs, Medical Devices
Recalls by year
12
13
14
19
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 14, 2021DrugsFDA
Kimberly-Clark Corporation recalls Scott¿ Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz), Distributed in the U.S. by Kimberly-Clark Global Sales
Hazard: Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are incorrectly labeled as Moisturizing Foam Hand Sanitizer
January 23, 2019Medical DevicesFDA
Kimberly-Clark Corporation recalls U by Kotex¿ Sleek¿, Regular Tampons, 3 Count
Hazard: Potential for tampon to come apart upon removal.
January 23, 2019Medical DevicesFDA
Kimberly-Clark Corporation recalls U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack
Hazard: Potential for tampon to come apart upon removal.
January 23, 2019Medical DevicesFDA
Kimberly-Clark Corporation recalls U by Kotex¿ Sleek¿, Regular Tampons, 34 Count
Hazard: Potential for tampon to come apart upon removal.
January 23, 2019Medical DevicesFDA
Kimberly-Clark Corporation recalls U by Kotex¿ Sleek¿, Regular Tampons, 18 Count
Hazard: Potential for tampon to come apart upon removal.
February 5, 2014Medical DevicesFDA
Kimberly-Clark Corporation recalls Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Ki
Hazard: Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.
December 25, 2013Medical DevicesFDA
Kimberly-Clark Corporation recalls Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usag
Hazard: Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7 mL Epilor plastic Luer-Lok LOR Syringes under recall by Becton Dickinson (BD) because the product may stall or stick when traveling within the barrel of the syringe.
April 3, 2013Medical DevicesFDA
Kimberly-Clark Corporation recalls KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose
Hazard: Some individual container filter units might contain thin areas that may potentially compromise the ability of the filter to maintain a sterile barrier.
December 5, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated
Hazard: Error 85 alarm on the Model 1000 Control Unit was occasionally triggered inappropriately.
November 14, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls MicroCool Breathable Gown with Towels, X-Larg, X-Long, Sterile The product is a sterile, single use, surgical gown in
Hazard: Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled.
November 14, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is a sterile, single use, surgical gown intended to
Hazard: Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled.
September 26, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgic
Hazard: The impacted product was not intended for commercial distribution to end users.
September 26, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls Kimberly-Clark MIC PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic gastro
Hazard: The placement guidewire diameter is too large and does not pass-through the introducer needle during the placement procedure of the PEG Feeding Tube.
September 26, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic
Hazard: The placement guidewire diameter is too large and does not pass-through the introducer needle during the placement procedure of the PEG Feeding Tube.
August 15, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls Kimberly Clark Patient Warming System - Model 1000 Control Unit. Kimberly Clark Patient Warming System - Model 1000
Hazard: A defect of the "fuse holder" can lead to a Control Unit failure that may cause the device to lose its ability to warm and maintain set temperature and may also result in excessive heat with the fuse assembly that could lead to the generation of smoke.
July 25, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls MicroCool Breathable Impervious Gown with Secure Fit Surgical, (Large and X-Large), Made in Honduras. The Kimberly Cl
Hazard: Complaints were received of gowns pilling or balling, linting and abrades, blood strikethrough and fibers falling off the gowns.
July 25, 2012Medical DevicesFDA
Kimberly-Clark Corporation recalls MicroCool Breathable Impervious Surgical Gown, (Large and X-Large), Sterile, Made in Honduras. The Kimberly Clark Mic
Hazard: Complaints were received of gowns pilling or balling, linting and abrades, blood strikethrough and fibers falling off the gowns.
July 18, 2012DrugsFDA
Kimberly-Clark Corporation recalls Kleenex Foam Hand Sanitizer, Alcohol Free in a) 1.5 fl oz. (45mL) , b) 8 fl oz. (236mL) , and c) 16 fl oz (473mL) bottle
Hazard: Microbial Contamination of Non-Sterile Products; The affected lots were found to be contaminated with bacterium, Burkholderia cepacia complex.
July 18, 2012DrugsFDA
Kimberly-Clark Corporation recalls Kleenex Luxury Foam Hand Sanitizer, (Benzalkonium Chloride 0.1%), in a) 1 Liter (33.8 fl oz.), b) 1.2 Liters (40.5 fl oz
Hazard: Microbial Contamination of Non-Sterile Products; The affected lots were found to be contaminated with bacterium, Burkholderia cepacia complex.