PlainRecalls

Kimberly-Clark Corporation

Compiled from official public sources by the publisher.

19 recalls on record · Latest: Apr 14, 2021

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Agency notice ledger

Federal filing book Kimberly-Clark Corporation LIGHT-BOOK · MULTI-AGENCY

#851 of 14,151 · 19 notices · 0.018% archive

  • BOOK 19 notices
  • RANK #851 of 14,151
  • SHARE 0.018% archive
  • AGENCY FDA Devices (16)
  • CAT medical devices
  • CATS 3 categories
  • LATEST Apr 14, 2021
  • PHOTO Abbott

Nearest notice-volume peer: Abbott (0 notice gap)

Kimberly-Clark Corporation accounts for about 0.018% of the 104,423-notice archive on 19 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Kimberly-Clark Corporation compares to 14,151 recalling firms

Kimberly-Clark Corporation ranks 851st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Kimberly-Clark Corporation vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

19 851st of 14151 higher than 13,281 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Kimberly-Clark Corporation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Kimberly-Clark Corporation holds about 0.018% of archive notices alongside 19 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026

How the 19 notices break down

Same federal filing book as the hero total — split by issuing agency, no new counts.

FDA Drug Moderate Apr 14, 2021

Scott¿ Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz), Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199 Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5 UPC 0 36000 91592 1
FDA Devices Moderate Jan 23, 2019

U by Kotex¿ Sleek¿, Regular Tampons, 3 Count
FDA Devices Moderate Jan 23, 2019

U by Kotex¿ Sleek¿, Regular Tampons, 18 Count
FDA Devices Moderate Jan 23, 2019

U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack
FDA Devices Moderate Jan 23, 2019

U by Kotex¿ Sleek¿, Regular Tampons, 34 Count
FDA Devices Moderate Feb 5, 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.
FDA Devices Moderate Dec 25, 2013

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
FDA Devices Moderate Apr 3, 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.
FDA Devices Moderate Dec 5, 2012

Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated for monitoring and controlling patient temperature.
FDA Devices Moderate Nov 14, 2012

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.
FDA Devices Moderate Nov 14, 2012

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.
FDA Devices Moderate Sep 26, 2012

Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic gastrostomy (PEG) tubes intended for a non-surgical "pull" endoscopic placement technique. The PEG tube is held in place during use with an external retention disk.
FDA Devices Moderate Sep 26, 2012

Kimberly-Clark MIC PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic gastrostomy (PEG) tubes intended for a non-surgical "pull" endoscopic placement technique. The PEG tube is held in place during use with an external retention disk.
FDA Devices Low Sep 26, 2012

ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown 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.
FDA Devices Moderate Aug 15, 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.
FDA Devices Moderate Jul 25, 2012

MicroCool Breathable Impervious Surgical Gown, (Large and X-Large), Sterile, Made in Honduras. The Kimberly Clark Micro COOL Surgical Gowns are sterile single use surgical apparel intended to be worn by heathcare professionals to help protect the patient and the healthcare worker from the transfer of microorganisms, body fluids and particulate matter.
FDA Devices Moderate Jul 25, 2012

MicroCool Breathable Impervious Gown with Secure Fit Surgical, (Large and X-Large), Made in Honduras. The Kimberly Clark Micro COOL Surgical Gowns are sterile single use surgical apparel intended to be worn by heathcare professionals to help protect the patient and the healthcare worker from the transfer of microorganisms, body fluids and particulate matter.
FDA Drug Moderate Jul 18, 2012

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.) Cassettes, Distributed by Kimberly Clark, LLC, Roswell, GA 30076
FDA Drug Moderate Jul 18, 2012

Kleenex Foam Hand Sanitizer, Alcohol Free in a) 1.5 fl oz. (45mL) , b) 8 fl oz. (236mL) , and c) 16 fl oz (473mL) bottles, Distributed by Kimberly Clark, LLC, Roswell, GA 30076

Kimberly-Clark Corporation holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (19 here).

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Adm Milling 19 Advance Pierre N 19

Similar medical devices volume

Nearest multi-notice firms that share this firm's dominant product category.

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Amo Puerto Rico Manufacturing, Inc. 19

Frequently Asked Questions

How many federal recall notices name Kimberly-Clark Corporation? ▼
PlainRecalls indexes 19 distinct federal recall events naming Kimberly-Clark Corporation, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Kimberly-Clark Corporation sit among other recalling firms? ▼
Kimberly-Clark Corporation ranks #851 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Kimberly-Clark Corporation's notices? ▼
FDA Devices accounts for 16 of this firm's 19 indexed notices across 2 issuing agencies.
What product category dominates Kimberly-Clark Corporation's filing book? ▼
Filings for Kimberly-Clark Corporation span 3 product categories, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Kimberly-Clark Corporation: 19 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Kimberly-Clark Corporation; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026