Equate ClearLAX Powder Recall: Unfiled NDC Numbers Risk Mislabeling
Lupin Somerset recalls Equate ClearLAX Polyethylene Glycol 3350 Powder due to unfiled NDC numbers on some bottles. This may lead to mislabeling and incorrect product identification.
Lower-risk recall
Labeling: Not Elsewhere Classified - A private label distributor noted unfiled NDC numbers on EQ ClearLax Polyethylene Glycol 3350 NF Powder Solution of various sizes.
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What happened, in plain English
Lupin Somerset is recalling Equate ClearLAX Polyethylene Glycol 3350 Powder for Solution bottles that have unfiled NDC numbers. This issue could lead to mislabeling, which might cause consumers to use the wrong product. Read more at govinfonow.com/recall/40450-equate-clearlax-powder-recall-unfiled-ndc-numbers-risk-mislabeling.
Source Summary by GovInfoNow · govinfonow.com/recall/40450-equate-clearlax-powder-recall-unfiled-ndc-numbers-risk-mislabeling · Updated October 7, 2026 · FDA enforcement record: FDA #D-0907-2018
Cite this page
“Equate ClearLAX Powder Recall: Unfiled NDC Numbers Risk Mislabeling.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40450-equate-clearlax-powder-recall-unfiled-ndc-numbers-risk-mislabeling. Based on FDA recall #D-0907-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0907-2018%22&limit=1).
Why it’s dangerous
The recall is due to unfiled NDC numbers on some bottles, which means the product may not be properly labeled. This could lead to mislabeling, where the product might be confused with another item, potentially causing incorrect usage.
Who’s affected
People who purchased Equate ClearLAX Polyethylene Glycol 3350 Powder for Solution in specific bottle sizes and with the listed NDC numbers from Walmart. Those most at risk are individuals using the product for laxative purposes who might receive mislabeled items.
How to tell if you have this one
Check for the following NDC numbers on the bottle: 49035-312-07 (119g), 49035-312-08 (238g), and specific batch codes like M16425A through S800453. These products were distributed by Walmart in the United States.
- Brand
Lupin Somerset- Category
Drug
What to do — step by step
Check Product Labels
Look for the NDC numbers listed in the recall notice to confirm if your bottle is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.6 years after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have this product?
Check the product labels for the specific NDC numbers listed in the recall notice. If your product matches, you may want to contact the manufacturer for further instructions.
Is there a risk of serious injury from this product?
The recall is for mislabeling risk, not a direct safety hazard. There is no indication of serious injury risk from the product itself.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0907-2018 (June 13, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0907-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.