Mckesson Medical-Surgical recalls 100mg Labetalol Hydrochloride Tablets (NDC 49884-122-01) due to potential temperature abuse. This could affect prescription safety.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling 100mg Labetalol Hydrochloride Tablets (100-count bottles) because of temperature abuse risks. This could lead to unsafe medication conditions if the product is exposed to improper temperatures.
The recall is due to cGMP deviations related to temperature abuse. This means the product may have been exposed to temperatures that could compromise its safety and effectiveness.
Prescription holders who received the specific product from Mckesson Medical-Surgical. Patients on blood pressure medication are most at risk if the tablets are improperly stored.
Check for the product name 'Labetalol Hydrochloride Tablets, USP, 100 mg, 100-count bottle' with NDC 49884-122-01. The product was distributed by Mckesson Medical-Surgical and is prescription-only.
Identify the product by checking the NDC code 49884-122-01 and the prescription label.
The recall indicates potential temperature abuse risks, so it is not safe to use without verification.
Check for the NDC code 49884-122-01 on the product label and confirm it was distributed by Mckesson Medical-Surgical.
The recall does not specify a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1094-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1094-2022 from Mckesson Medical-Surgical. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
