Woodbine Products Antibacterial Foaming Wash with Hydria Recall

Why it was recalled

Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.

Product description

Antibacterial Foaming Wash with Hydria Moisturizing Formula, Cucumber-Melon Scent, 1250 mL (42 fl oz.), Manufactured for: Triple S, 800-323-2251, Made in USA, NDC 11429-1010-8

Lot numbers, UPCs & expiration codes

Lot #: VDAF017, Exp 4/24; VDAF018, Exp 5/24

Where it was sold

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-0006-2023
Classification: Class III
Status: Terminated
Recall initiated: Aug 30, 2022
FDA report date: Oct 12, 2022
Quantity: 595 cases (4 bottles per case)
Recall type: Voluntary: Firm initiated
Recalling firm: Woodbine Products Co Inc

Original FDA data

Every field from FDA enforcement report D-0006-2023, exactly as published.

Show all FDA fields

City: Medina
State: OH
Status: Terminated
Country: United States
Event ID: 90846
Address: 915 W Smith Rd
Code information: Lot #: VDAF017, Exp 4/24; VDAF018, Exp 5/24
Postal code: 44256-2446
Report date: Oct 12, 2022
Product type: Drugs
Recall number: D-0006-2023
Classification: Class III
Recalling firm: Woodbine Products Co Inc
Product quantity: 595 cases (4 bottles per case)
Termination date: Sep 28, 2023
Reason for recall: Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Antibacterial Foaming Wash with Hydria Moisturizing Formula, Cucumber-Melon Scent, 1250 mL (42 fl oz.), Manufactured for: Triple S, 800-323-2251, Made in USA, NDC 11429-1010-8
Distribution pattern: NC
Recall initiation date: Aug 30, 2022
Initial firm notification: Telephone
Center classification date: Oct 6, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0006-2023, published Oct 12, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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