Antibacterial Hand Wash Recalled for Incorrect Scent Label
Woodbine Products is recalling FOAMFRESH DYE FREE ANTIBACTERIAL HAND WASH due to incorrect scent information on the label. The affected lots VDAF017 and VDAF018 were distributed in North Carolina, and no illnesses have been reported.
The agency’s classification
FDA (Drugs): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: This is an FDA Class III recall involving only a labeling error. Per the severity rubric, cosmetic defects and documentation issues constitute Low severity, particularly when no safety hazard or illnesses are reported.
Plain-English summary
Woodbine Products Co Inc is recalling FOAMFRESH DYE FREE ANTIBACTERIAL HAND WASH (Chloroxylenol), a 1250 mL foaming hand wash, because the label lists incorrect information about the product's scent. The label does not accurately identify the actual scent of the product.
The recalled products are identified by Lot #VDAF017 (expiration 4/24) and Lot #VDAF018 (expiration 5/24). A total of 595 cases (4 bottles per case) were distributed in North Carolina.
No illnesses or injuries have been reported in connection with this product. Consumers who purchased the affected lots should verify the lot number on their bottle. For additional information, contact Woodbine Products Co Inc at 800-323-2251.
The recalled product
- Product
- FOAMFRESH DYE FREE ANTIBACTERIAL HAND WASH (CHLOROXYLENOL)
- Brand
- FOAMFRESH DYE FREE ANTIBACTERIAL HAND WASH
- Manufacturer
- Woodbine Products Co Inc
- Category
- Drug — Topical
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Lot #: VDAF017
- Exp 4/24
- VDAF018
- Exp 5/24
Distribution
Distributed in 1 state:
Related recalls
Same hazard · mis labeling
See all →- SevereImperio Distribution Recalls Beef Jerky Produced Without Federal Inspection
USDA FSIS · 2026-10-24
- LowMagellan LeadCare II Blood Lead Test Kit Recall for Labeling Error
FDA (Devices) · 2026-10-21
- ModerateIn2bones Recalls Partially Threaded Bone Screws Due to Labeling Error
FDA (Devices) · 2026-10-21
- SevereInstrumentation Laboratory Recalls HemoslL AcuStar HIT-lgG In Vitro Diagnostic Reagents
FDA (Devices) · 2026-10-21
- SevereDeano's Pasta Recalls Pear and Pecorino Ravioli for Undeclared Lobster
FDA (Food) · 2026-10-21
Similar recalls
- ModerateEcolab Recalls Medi-Stat Foam Hand Soap Due to Labeling Error
FDA (Drugs) · 2018-11-28
- ModerateFDA Recalls PROBLEND Hand Sanitizer for Manufacturing Deviations
FDA (Drugs) · 2024-03-06
- ModerateSteris Recalls Kindest Kare Antimicrobial Foaming Handwash Due to Labeling Error
FDA (Drugs) · 2015-12-16
- HighArray Liquid Antiseptic Handwash Recalled for Microbiological Test Failures
FDA (Drugs) · 2024-12-11
- SevereLeafree Hand Sanitizer Recalled for Lacking FDA Approval
FDA (Drugs) · 2020-09-30
- HighFoaming Hand Sanitizer Recalled for Elevated Acetaldehyde and Acetal Levels
FDA (Drugs) · 2023-05-31