Rootify
CompaniesFAQ
Baby WipesKimberly-Clark Worldwide, Inc.

Huggies Ultimate Skin Protect Wipes 64 Pack

Barcode
What is in it
Not published
No ingredient list was found in any source we check.
Open research
Not disclosed
No ingredient list was found in any source we check, as of 2026-09-27.
Recalls
No recalls
No government notice we hold lists this product.
Certified organic
Doesn't apply
Organic certification does not apply to this kind of product.
Non-GMO verified
Not verified
Not verified by any public database
Who owns the brand
Kimberly-Clark Worldwide, Inc.
Kimberly-Clark Worldwide, Inc..

Each row says what a public record says, never whether a product is good. What each answer means.

Every source and date for this page →
IngredientsIn label order
No ingredient list was found in any source we check, as of 2026-09-27.
No flagged ingredientsiNothing flagged
No ingredient list was found in any source we check, as of 2026-09-27.
7 recalls and government noticesFDA, FSIS, CPSC and CBP records
Notices that list this product0

No government notice we hold lists this product.

Notices naming Kimberly-Clark Worldwide, Inc., without naming this product7
FDA · Class II2013-10-29Terminated

Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.

What it covered: 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.

Issued by Kimberly-Clark Worldwide, Inc.. The notice named “KIMBERLY CLARK”. It covers the product described, not necessarily every product of this brand.

FDA · Class II2013-10-24Terminated

May contain small pieces of plastic.

The notice says: 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.

What it covered: 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

Issued by Kimberly-Clark Worldwide, Inc.. The notice named “KIMBERLY CLARK”. It covers the product described, not necessarily every product of this brand.

FDA · Class II2012-04-27Terminated

May contain too much lead.

The notice says: 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.

What it covered: 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.

Issued by Kimberly-Clark Worldwide, Inc.. The notice named “KIMBERLY CLARK”. It covers the product described, not necessarily every product of this brand.

FDA · Class III2010-12-31Terminated

The impacted product was not intended for commercial distribution to end users.

What it covered: 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.

Issued by Kimberly-Clark Worldwide, Inc.. The notice named “KIMBERLY CLARK”. It covers the product described, not necessarily every product of this brand.

FDA · Class II2010-09-16Terminated

Error 85 alarm on the Model 1000 Control Unit was occasionally triggered inappropriately.

What it covered: Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated for monitoring and controlling patient temperature.

Issued by Kimberly-Clark Worldwide, Inc.. The notice named “KIMBERLY CLARK”. It covers the product described, not necessarily every product of this brand.

FDA · Class II2010-06-22Terminated

May contain small pieces of something that should not be in food.

The notice says: The placement guidewire diameter is too large and does not pass-through the introducer needle during the placement procedure of the PEG Feeding Tube.

What it covered: 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.

Issued by Kimberly-Clark Worldwide, Inc.. The notice named “KIMBERLY CLARK”. It covers the product described, not necessarily every product of this brand.

The agency filed 2 records under this notice, one per affected product line.

FDA · Class II2009-09-17Terminated

Complaints were received of gowns pilling or balling, linting and abrades, blood strikethrough and fibers falling off the gowns.

What it covered: 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.

Issued by Kimberly-Clark Worldwide, Inc.. The notice named “KIMBERLY CLARK”. It covers the product described, not necessarily every product of this brand.

The agency filed 2 records under this notice, one per affected product line.

Every notice above — sources and dates