Wise Pharmacy recalls 15mL Acetylcysteine 2% Otic Drops (Rx only) due to lack of processing controls. Compounded in Littleton, CO. Check lot number 7131N (exp 7/11/19) for affected units.
Lack of Processing Controls
Wise Pharmacy is recalling 15mL Acetylcysteine 2% Otic Drops (prescription-only) because of processing control issues. This could lead to unsafe medication if not handled properly. Affected units were compounded in Littleton, CO with lot number 7131N expiring July 2019.
The recall is due to 'Lack of Processing Controls' which means the medication may not have been prepared safely. This could result in incorrect concentrations or contamination, potentially causing harm if used without proper care.
Prescription holders who received the 15mL Acetylcysteine 2% Otic Drops compounded by Wise Pharmacy in Littleton, CO. People using the product for ear infections may be at risk if the medication was improperly processed.
Check for the 15mL bottle labeled 'Acetylcysteine 2% Otic Drop, Rx only'. The product was compounded by Wise Pharmacy in Littleton, CO with lot number 7131N (expiring July 11, 2019).
Look for the lot number 7131N on the bottle label, which expires July 11, 2019.
The recall states there is a lack of processing controls, so the product may not be safe. Do not use until the recall remedy is followed.
The recall remedy is not stated in the record, so no specific action is required beyond checking the lot number.
Check for the lot number 7131N on the bottle label, which was compounded by Wise Pharmacy in Littleton, CO and expires July 11, 2019.
We’ve drafted a message you can send Wise Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-1567-2019 — Wise Pharmacy Wise Pharmacy Hello, I own a Wise Pharmacy that is covered by recall D-1567-2019 from Wise Pharmacy. 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.
