H J Harkins Company Inc dba Pharma Pac recalls Valsartan tablets 160 mg, 90-count bottle, Rx Only, Repackaged by H.J. Harkins Co, Inc. Grover Beach, CA 93433, NDC
Carcinogen impurity detected in API used to manufacture drug product.
Recall notice
Carcinogen impurity detected in API used to manufacture drug product.
Contact the company & request your remedy
We’re still writing up this recall
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/39845-h-j-harkins-company-inc-dba-pharma-pac-recalls-valsartan · Recall date July 26, 2018 · FDA enforcement record: FDA #D-1022-2018
Cite this page
“H J Harkins Company Inc dba Pharma Pac recalls Valsartan tablets 160 mg, 90-count bottle, Rx Only, Repackaged by H.J. Harkins Co, Inc. Grover Beach, CA 93433, NDC.” GovInfoNow, recall dated July 26, 2018. https://govinfonow.com/recall/39845-h-j-harkins-company-inc-dba-pharma-pac-recalls-valsartan. Based on FDA recall #D-1022-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1022-2018%22&limit=1).
How to tell if you have this one
- Brand
H J Harkins Company Inc dba Pharma Pac- Category
Drug
Contact H J Harkins Company Inc dba Pharma Pac
We’ve drafted a message you can send H J Harkins Company Inc dba Pharma Pac to request your refund or repair — edit it as you like.
Subject: Recall D-1022-2018 — H J Harkins Company Inc dba Pharma Pac H J Harkins Company Inc dba Pharma Pac recalls Valsartan tab Hello, I own a H J Harkins Company Inc dba Pharma Pac recalls Valsartan tablets 160 mg, 90-count bottle, Rx Only, Repackaged by H.J. Harkins Co, Inc. Grover Beach, CA 93433, NDC that is covered by recall D-1022-2018 from H J Harkins Company Inc dba Pharma Pac. 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-1022-2018 (July 26, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1022-2018 to see it in context.
- 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.