Pharmaceutical Associates recalls Cimetidine Hydrochloride Oral Solution 300 mg/5 mL (8 fl oz) due to potential carryover of Senna Syrup. This Rx-only medication may pose a risk if used incorrectly.
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Pharmaceutical Associates is recalling a prescription-only cimetidine oral solution because it might carry over senna syrup during manufacturing. This could lead to unintended medication interactions if the product is used without proper care.
The recall is triggered by a potential carryover of senna syrup during manufacturing. This could cause unintended medication interactions if the product is used without proper care, especially since it's a prescription-only medication.
Prescription patients who received this specific cimetidine solution from Pharmaceutical Associates. Those using the product without medical supervision are at higher risk due to the potential for medication interactions.
Check for the product name 'Cimetidine Hydrochlor: 300 mg/5 mL, 8 fl oz (237 mL)' with NDC 0121-0649-08 and lot number C62F expiring October 31, 2022. This medication is only available by prescription.
Verify the product label includes NDC 0121-0649-08 and lot number C62F expiring October 31, 2022.
The product is prescription-only and may pose a risk of medication interactions if senna syrup carries over. Consult your healthcare provider before use.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to use the product.
Check the product label for NDC 0121-0649-08 and lot number C62F expiring October 31, 2022. This medication is only available by prescription.
We’ve drafted a message you can send Pharmaceutical Associates to request your refund or repair — edit it as you like.
Subject: Recall D-0722-2021 — Pharmaceutical Associates Pharmaceutical Associates Hello, I own a Pharmaceutical Associates that is covered by recall D-0722-2021 from Pharmaceutical Associates. 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.
