Unichem Pharmaceuticals USA recalls 0.3mg Clonidine Hydrochloride Tablets due to possible mix-up with 0.2mg strength. This could lead to incorrect dosing if used without medical supervision.
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
Unichem Pharmaceuticals is recalling 0.3 mg Clonidine Hydrochloride Tablets because some bottles may contain the wrong strength (0.2 mg instead of 0.3 mg). This mix-up could cause incorrect dosing if taken without medical guidance.
The product may contain 0.2 mg tablets instead of the labeled 0.3 mg strength. This mix-up could lead to incorrect dosing if the medication is taken without medical supervision, potentially causing under-treatment or over-treatment.
People who have the 0.3 mg Clonidine Hydrochloride Tablets (100-count bottle) from Unichem Pharmaceuticals USA. Those with medical conditions requiring precise dosing are at higher risk.
Check for the product name 'Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle' on the label. The NDC code is 29300-137-01 and lot number GCLH22005 (expiring 02/29/2024).
Look for the NDC code 29300-137-01 and lot number GCLH22005 on the label to confirm it's the recalled item.
The product may contain the wrong strength (0.2 mg instead of 0.3 mg), so it should not be used without medical supervision.
Check for the NDC code 29300-137-01 and lot number GCLH22005 on the label.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to use the product.
We’ve drafted a message you can send Unichem Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1541-2022 — Unichem Pharmaceuticals Unichem Pharmaceuticals Hello, I own a Unichem Pharmaceuticals that is covered by recall D-1541-2022 from Unichem 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.
