Winder Laboratories recalls 100-count Phenazopyridine HCl tablets USP 100 mg bottles due to accidental mix-up with phenobarbital tablets. Consumers should check product details and contact the manufacturer for guidance.
Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.
Winder Laboratories is recalling 100-count bottles of Phenazopyridine HCl tablets USP 100 mg (Rx only) because they accidentally mixed up with phenobarbital tablets. This mix-up could lead to taking the wrong medication, which may cause serious health issues.
The recall is for a product mix-up where a bottle of Phenazopyridine HCl tablets USP 100 mg accidentally contained Phenobarbital tablets 16.2 mg. Phenobarbital is a different medication that can cause serious health risks if taken instead of phenazopyridine.
People who have the 100-count bottles of Phenazopyridine HCl tablets USP 100 mg (Rx only) from Winder Laboratories are affected. Those who may have taken the phenobarbital tablets instead of phenazopyridine could be at risk.
Check for the product name 'Phenazopyridine HCl Tablets USP 100 mg', 100-count bottles, manufactured by Winder Laboratories, LLC, with NDC 75826-114-10 and lot number 1142404.
Look for the NDC code 75826-114-10 and lot number 1142404 on the bottle to confirm if it's part of the recall.
The product was recalled because a bottle of Phenazopyridine HCl tablets USP 100 mg accidentally contained Phenobarbital tablets 16.2 mg.
Check the product details for the NDC code 75826-114-10 and lot number 1142404. Contact Winder Laboratories for further guidance.
The recall record does not specify the risk level, so it's unknown if serious injury could occur.
We’ve drafted a message you can send Winder Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0545-2024 — Winder Laboratories Winder Laboratories Hello, I own a Winder Laboratories that is covered by recall D-0545-2024 from Winder Laboratories. 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.
