Kimberly-Clark Corporation
Kimberly-Clark Corporation holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2023, with 16 FDA device recalls on record.
Name variants for Kimberly-Clark Corporation
as filed with FDA- Kimberly-Clark Corporation
- Kimberly Clark Corporation
Top product codes for Kimberly-Clark Corporation
FDA recalls by Kimberly-Clark Corporation
10 most recent of 16- Z-0748-2019 — U by Kotex¿ Sleek¿, Regular Tampons, 18 Count
- Z-0749-2019 — U by Kotex¿ Sleek¿, Regular Tampons, 34 Count
- Z-0750-2019 — U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack
- Z-0751-2019 — U by Kotex¿ Sleek¿, Regular Tampons, 3 Count
- Z-0850-2014 — Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Kimberly-Clark,Product code PMF22-100-10 The product is used to create lesions in nervous tissue when used with the Kimberly-Clark radiofrequency generator and probes.
- Z-0518-2014 — Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage: The device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs
- Z-0995-2013 — KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose another medical device that is to be sterilized by a health care provider.
- Z-0258-2013 — MicroCool Breathable Gown with Towels, X-Larg, X-Long, Sterile The product is a sterile, single use, surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material.
- Z-0257-2013 — ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is a sterile, single use, surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material.
- Z-2181-2012 — Kimberly Clark Patient Warming System - Model 1000 Control Unit. Kimberly Clark Patient Warming System - Model 1000 Control Unit and Energy Transfer Pads is a thermal regulating system, indicated for monitoring and controlling patient temperature.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Kimberly-Clark Corporation
- K231435 — KIMTECH Polaris Xtra Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid and Fentanyl in Simulated Gastric Acid
- K231021 — KIMTECH Polaris Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid and Fentanyl in Simulated Gastric Acid
- K223749 — U by Kotex® Click® Unscented Menstrual Tampons
- K202416 — Kimtech Prizm Multi-Layered Exam Glove Tested for use with Chemotherapy Drugs, the Opioid Fentanyl Citrate, simulated Gastric Acid, and Fentanyl in Gastric Acid, Kimtech Prizm Xtra Multi-Layered Exam Glove Tested for use with Chemotherapy Drugs, the Opioid Fentanyl Citrate, simulated Gastric Acid, and Fentanyl in Gastric Acid
- K200072 — KIMTECH Purple Nitrile Powder Free Examination Gloves Tested for Use with Chemotherapy Drugs, the Opioid Fentanyl, Gastric acid, and Fentanyl in Gastric acid
- K172118 — U by Kotex Click Unscented Menstrual Tampons
- K143164 — ON-Q Pain Relief System, QuikBloc Over-the-Needle Catheter Set
- K140539 — AERO BLUE PERFORMANCE SURGICAL GOWN
- K122653 — MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES
- K120650 — POISE PERSONAL LUBRICANT
- K113333 — KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS
- K113036 — U BY KOTEX CLICK UNSCENTED MENSTRUAL TAMPONS
- K103311 — U BY KOTEX CLICK UNSCENTED MENSTRUL TAMPONS
Data sourced from openFDA. This site is unofficial and independent of the FDA.