Granules Pharmaceuticals recalls 0.6 mg Colchicine Capsules 30-count bottles (Rx only) manufactured in 2015 with lot #GPC240763B due to failed dissolution specifications during stability testing.
Failed Dissolution Specifications: Out of specification observed during the accelerated stability conditions for the 30 count bottles.
Granules Pharmaceuticals is recalling 0.6 mg Colchicine Capsules 30-count bottles (Rx only) because they failed dissolution tests during stability testing. This could affect medication reliability if used as prescribed.
The capsules failed dissolution tests during accelerated stability testing, meaning they may not release the medication correctly when taken. This could lead to inconsistent dosing if used as prescribed.
Prescription patients who received these specific Colchicine Capsules from Granules Pharmaceuticals in 2015. Those with medical conditions requiring Colchicine may be at higher risk if the medication doesn't dissolve properly.
Check for 0.6 mg Colchicine Capsules 30-count bottles labeled 'Rx only' with manufacturer code NDC 70010-001-03 and lot number GPC240763B. These were manufactured in 2015 and expire June 17, 2026.
Verify the product label includes NDC 70010-001-03 and lot number GPC240763B for the recalled capsules.
The recall is due to failed dissolution tests during stability testing, not immediate safety concerns. Patients should consult their doctor if they have concerns about medication reliability.
Check for NDC 70010-001-03 and lot number GPC240763B on the product label. These capsules were manufactured in 2015 and expire June 17, 2026.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to continue using the product.
We’ve drafted a message you can send Granules Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0187-2025 — Granules Pharmaceuticals Granules Pharmaceuticals Hello, I own a Granules Pharmaceuticals that is covered by recall D-0187-2025 from Granules Pharmaceuticals. 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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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.
