KIMBERLY-CLARK CORPORATION Cold Spring
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (1)
Devices registered here (1)
- Pad, Menstrual, UnscentedProduct code HHD (opens in a new tab) · Class I · Obstetrics/Gynecology · 21 CFR 884.5435
Recalls & enforcement
- Class IITerminated2018-12-11Potential for tampon to come apart upon removal.
FDA inspections (1)
- VAI2019-07-25Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
- All facilities operated by KIMBERLY-CLARK CORPORATION
- KIMBERLY-CLARK CORPORATION (WI)
- Kimberly-Clark Vietnam Ltd. (VN)
- K-C AFC Manufacturing, S. de R.L. de C.V (MX)
- Kimberly-Clark Inc. (CA)
- KIMBERLY-CLARK CORPORATION PARIS PLANT (TX)
- Kimberly-Clark Corporation (UT)
- KIMBERLY-CLARK CORPORATION (BEECH ISLAND MILL) (SC)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “KIMBERLY-CLARK CORPORATION Cold Spring (FEI 1000139864) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000139864-kimberly-clark-corporation-cold-spring/
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