Amerisource Health Services Paricalcitol Capsules Recall: Failed Impurities Risk
Amerisource Health Services recalls Paricalcitol Capsules (1 mcg, 30 capsules) due to failed impurities tests. This medication is prescription-only and may pose safety risks if impurities are present.
Recall notice
Failed Impurities/Degradation Specifications: This repackaged product was recalled by its manufacturer due to failed results for impurities.
Contact the company
What happened, in plain English
Amerisource Health Services has recalled Paricalcitol Capsules (1 mcg, 30 capsules) because the product failed impurities and degradation tests. This recall is for prescription-only medication that could pose safety risks if impurities are present. Read more at govinfonow.com/recall/42303-amerisource-health-services-paricalcitol-capsules-recall-failed-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/42303-amerisource-health-services-paricalcitol-capsules-recall-failed-impurities-risk · Updated October 9, 2026 · FDA enforcement record: FDA #D-0009-2017
Cite this page
“Amerisource Health Services Paricalcitol Capsules Recall: Failed Impurities Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42303-amerisource-health-services-paricalcitol-capsules-recall-failed-impurities-risk. Based on FDA recall #D-0009-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0009-2017%22&limit=1).
Why it’s dangerous
The product failed impurities and degradation specifications, meaning it may contain harmful substances not supposed to be in the medication. This could lead to safety issues for patients taking the medication.
Who’s affected
Prescription patients who have this specific Paricalcitol Capsule product are affected. Those with medical conditions requiring this medication are at higher risk.
How to tell if you have this one
Check for Paricalcitol Capsules (1 mcg, 30 capsules) with NDC 60687-106-25 or 60687-106-95. The product was distributed by American Health Packaging and has a lot number of 154341 with an expiration date of March 2017.
- Brand
Amerisource Health Services- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC 60687-106-25 or 60687-106-95 on the blister card or packaging.
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 9 months 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.
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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-0009-2017 (September 30, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0009-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.