Hetero Labs, Ltd. - Unit III recalls Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway,
Hetero Labs recalls 145mg fenofibrate tablets (Rx only) due to foreign valacyclovir tablets in some bottles. Consumers should check NDC 31722-596-90 and lot E181370.
Lower-risk recall
Presence of Foreign Tablet/Capsule: A foreign identified as Valacyclovir tablet 500 mg was co-mingled in a bottle containing Fenofibrate Tablets, USP 145 mg.
Contact the company & request your remedy
What happened, in plain English
Hetero Labs is recalling fenof: 145mg tablets (Rx only) because some bottles contain foreign valacyclovir tablets. This could cause incorrect medication use if taken by mistake. Read more at govinfonow.com/recall/39570-hetero-labs-fenofibrate-tablets-recall-foreign-valacyclovir-tablet-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39570-hetero-labs-fenofibrate-tablets-recall-foreign-valacyclovir-tablet-risk · Updated October 6, 2026 · FDA enforcement record: FDA #D-1211-2018
Cite this page
“Hetero Labs Fenofibrate Tablets Recall: Foreign Valacyclovir Tablet Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39570-hetero-labs-fenofibrate-tablets-recall-foreign-valacyclovir-tablet-risk. Based on FDA recall #D-1211-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1211-2018%22&limit=1).
Why it’s dangerous
Foreign valacyclovir tablets (500mg) were accidentally mixed with fenofibrate tablets in some bottles. If someone takes the foreign tablets instead of the prescribed fenofibrate, they could receive an incorrect medication.
Who’s affected
People with prescriptions for fenofibrate who received this specific product. Those taking fenofibrate without knowing the foreign tablets could be at risk of taking the wrong medication.
How to tell if you have this one
Check for NDC code 31722-596-90 and lot number E181370 on the bottle. This product was manufactured for Camber Pharmaceuticals in Piscataway, NJ.
- Brand
Hetero Labs- Category
Drug
What to do — step by step
Check Product Label
Look for NDC 31722-596-90 and lot E181370 on the bottle.
Questions people ask
Is this product safe to use?
The recall is for specific bottles with foreign tablets; other bottles may be safe. Check the label for NDC 31722-596-90 and lot E181370.
What should I do if I have this product?
Check the label for NDC 31722-596-90 and lot E181370. If it matches, contact Hetero Labs for instructions.
Is there a risk of serious injury?
The recall is for incorrect medication use, not physical injury. This is a low-risk situation.
Contact Hetero Labs
We’ve drafted a message you can send Hetero Labs to request your refund or repair — edit it as you like.
Subject: Recall D-1211-2018 — Hetero Labs Hetero Labs Hello, I own a Hetero Labs that is covered by recall D-1211-2018 from Hetero Labs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1211-2018 (September 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1211-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.