CLASS III Drug recall · Reported 12 Oct 2022 · FDA Enforcement Report
Antibacterial Foaming Wash with Hydria Moisturizing Formula recalled
Woodbine Products is recalling Antibacterial Foaming Wash with Hydria Moisturizing Formula, Cucumber-Melon Scent, distributed in North Carolina. The recall was initiated on 30 Aug 2022 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0006-2023
- FDA event ID
- 90846
- Recalling firm
- Woodbine Products, Medina, OH
- Manufacturer
- Woodbine Products Company
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 30 Aug 2022
- FDA classified
- 6 Oct 2022
- Reported
- 12 Oct 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Labeling Errors
Timeline
| 30 Aug 2022 | Recall initiated by company | |
| 6 Oct 2022 | Classified by FDA | +37 days |
| 12 Oct 2022 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.
Product as listed by the FDA
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
Where it was distributed
NC
Questions about this recall
Why was it recalled?
Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.
Which lots are affected?
Lot #: VDAF017, Exp 4/24; VDAF018, Exp 5/24
Where was it sold?
NC
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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