Ascent Pharmaceuticals recalls 100-count hydrocodone/acetaminophen tablets due to product mix-up. This Rx-only medication may contain incorrect ingredients. Consumers should contact the manufacturer for details.
Product Mix-up
Ascent Pharmaceuticals is recalling 100-count hydrocodone bitartrate and acetaminophen tablets (10 mg/325 mg) that were manufactured for Camber Pharmaceuticals. The recall is due to a product mix-up, meaning the tablets might contain incorrect ingredients. This is a prescription-only medication that could pose risks if the wrong medication is taken.
The product mix-up means the tablets could contain incorrect ingredients. This could lead to taking the wrong medication, which might cause adverse effects. Since this is a prescription-only drug, patients should be cautious about the medication they receive.
Prescription patients who have the 100-count bottle of hydrocodone bitartrate and acetaminophen tablets (10 mg/325 mg) with lot number 21070817. People who take this medication for pain relief are most at risk if they receive the wrong product.
Check for the 100-count bottle labeled 'Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg'. Look for the lot number 21070817 on the packaging. This product was manufactured for Camber Pharmaceuticals and sold through prescription.
Verify the product label includes the lot number 21070817 and the manufacturer information for Camber Pharmaceuticals.
The recall is due to a product mix-up, so the tablets might contain incorrect ingredients. It is not safe to use without confirming the correct product.
The recall does not specify a remedy, so contact Ascent Pharmaceuticals directly for guidance.
Look for the lot number 21070817 on the packaging. This product was manufactured for Camber Pharmaceuticals and sold through prescription.
We’ve drafted a message you can send Ascent Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0276-2022 — Ascent Pharmaceuticals Ascent Pharmaceuticals Hello, I own a Ascent Pharmaceuticals that is covered by recall D-0276-2022 from Ascent 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.
