CLASS III Drug recall · Reported 28 Dec 2016 · FDA Enforcement Report
Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick recalled
Les Emballages Knowlton is recalling Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick, distributed nationwide in the US. The recall was initiated on 22 Nov 2016 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-0225-2017
- FDA event ID
- 75791
- Recalling firm
- Les Emballages Knowlton, Knowlton, N/A
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 22 Nov 2016
- FDA classified
- 22 Dec 2016
- Reported
- 28 Dec 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Drug class
- Sunscreen & Personal Care
Timeline
| 22 Nov 2016 | Recall initiated by company | |
| 22 Dec 2016 | Classified by FDA | +30 days |
| 28 Dec 2016 | 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: Label Mix Up- Incorrect back label applied to the product.
Product as listed by the FDA
Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick, Distributed by: Tom's of Maine, Kennebunk, ME 04043, Made in Canada, Unit UPC: 077326831953 Case UPC: 10077326831950
Where it was distributed
Nationwide
Questions about this recall
Is Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick recalled?
Yes. Les Emballages Knowlton recalled Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick on 22 Nov 2016. The recall is Class III and its status is Terminated. Recall number D-0225-2017.
Why was it recalled?
Labeling: Label Mix Up- Incorrect back label applied to the product.
Which lots are affected?
Lot: 6282CA3818 Exp: 10/18
Where was it sold?
Nationwide
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.