Lupin Pharmaceuticals Inc. recalls Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs
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Source Page by GovInfoNow · govinfonow.com/recall/40717-lupin-pharmaceuticals-inc-recalls-lupin-cefdinir-powder-for-oral-suspension · Recall date March 27, 2018 · FDA enforcement record: FDA #D-0684-2018
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“Lupin Pharmaceuticals Inc. recalls Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs.” GovInfoNow, recall dated March 27, 2018. https://govinfonow.com/recall/40717-lupin-pharmaceuticals-inc-recalls-lupin-cefdinir-powder-for-oral-suspension. Based on FDA recall #D-0684-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0684-2018%22&limit=1).
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We’ve drafted a message you can send Lupin Pharmaceuticals Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0684-2018 — Lupin Pharmaceuticals Inc. Lupin Pharmaceuticals Inc. recalls Lupin Cefdinir powder for Oral Suspen Hello, I own a Lupin Pharmaceuticals Inc. recalls Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs that is covered by recall D-0684-2018 from Lupin Pharmaceuticals Inc.. 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-0684-2018 (March 27, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0684-2018 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.