WipeEssentials Wet Wipes Recalled for Poor Quality Water
Diamond Wipes International is recalling WipeEssentials Wet Wipes because they were manufactured with poor quality water.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
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 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a manufacturing deviation (poor quality water) without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Diamond Wipes International, Inc. is recalling WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches. The recall involves 5,148,792 pouches distributed nationwide in the USA.
The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations, specifically that the finished products were manufactured with poor quality water.
Consumers should stop using the affected products and follow instructions from the recalling firm or the FDA for disposal or return.
The recalled product
- Product
- WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist. by Diamond Wipes Int'l, Inc., Chino, CA 91710, UPC 7 66670 03988 6.
- Manufacturer
- Diamond Wipes International, Inc.
- Affected units
- 5,148,792
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 (20)
- Lot #: 7382A1
- 7382B1
- 7382A2
- 7382B2
- 7382A3
- 7383A1
- 7383B1
- 7383A2
- 7401A1
- 7401B1
- 7572A1
- 7572B1
- 7577B1
- 7577A2
- 7577B2
- EXP 03/18
- 7573B1
- 7573A2
- 7782A1
- 7783A1
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Diamond Wipes International, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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