Mckesson Packaging Services recalls Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By:
Mckesson recalls 180mg Diltiazem CD capsules with failed dissolution testing. This may cause inconsistent drug release. Check NDC 63739-284-10 and lot 0114214 for affected products.
Recall notice
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Contact the company & request your remedy
What happened, in plain English
Mckesson is recalling 180mg Diltiazem CD capsules that failed dissolution testing. This could lead to inconsistent drug release, potentially affecting how the medication works. The recall applies to prescription-only bottles with specific NDC and lot numbers. Read more at govinfonow.com/recall/40604-mckesson-diltiazem-cd-180mg-recall-failed-dissolution-testing.
Source Summary by GovInfoNow · govinfonow.com/recall/40604-mckesson-diltiazem-cd-180mg-recall-failed-dissolution-testing · Updated October 7, 2026 · FDA enforcement record: FDA #D-0715-2018
Cite this page
“Mckesson Diltiazem CD 180mg Recall: Failed Dissolution Testing.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40604-mckesson-diltiazem-cd-180mg-recall-failed-dissolution-testing. Based on FDA recall #D-0715-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0715-2018%22&limit=1).
Why it’s dangerous
The capsules failed dissolution testing, meaning they may release medication too quickly or inconsistently. This could lead to ineffective treatment or unexpected side effects. However, the recall does not specify if this causes serious harm in normal use.
Who’s affected
Prescription holders of the 180mg Diltiazem CD capsules with NDC 63739-284-10 and lot 0114214 are affected. Patients taking this medication for blood pressure or chest pain are most at risk.
How to tell if you have this one
Check for the NDC code 63739-284-10 and lot number 0114214 on the bottle. These capsules are prescription-only and sold by Mckesson Packaging Services.
- Brand
Mckesson Packaging Services- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Nationwide with the US
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0714-2018 | Diltiazem HCl Extended-Release Capsules, USP 120 mg, 100-count bottles, Rx only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-014-10; Lot #: 0115086, Exp. 12/2018 | 4266 cartons |
| D-0715-2018 | Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10; Lot #: 0114214, Exp. 09/2018 | 7656 cartons |
| D-0716-2018 | Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-016-10; Lot #: 0115087, Exp. 12/2018 | 2966 cartons |
What to do — step by step
Check Product Details
Look for NDC 63739-284-10 and lot 0114214 on the bottle label.
Questions people ask
Is this product safe to use?
The recall states the capsules failed dissolution testing, but does not specify if they cause serious harm. The manufacturer has not provided a remedy, so it's best to check with your doctor.
What should I do if I have this product?
The recall does not provide a remedy, so contact your doctor or pharmacist for advice on whether to continue using the product.
How can I confirm if I have the recalled product?
Check the bottle for NDC 63739-284-10 and lot number 0114214. These capsules are prescription-only and sold by Mckesson Packaging Services.
Contact Mckesson Packaging Services
We’ve drafted a message you can send Mckesson Packaging Services to request your refund or repair — edit it as you like.
Subject: Recall D-0715-2018 — Mckesson Packaging Services Mckesson Packaging Services Hello, I own a Mckesson Packaging Services that is covered by recall D-0715-2018 from Mckesson Packaging Services. 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-0715-2018 (April 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0715-2018 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.