Mckesson recalls Verapamil HCL ampules due to temperature abuse risks. Patients with prescriptions should check if their product was affected by improper storage conditions.
cGMP deviations: Temperature abuse
Mckesson is recalling Verapamil HCL ampules that may have been exposed to improper temperatures. This could lead to unsafe drug concentrations if the product was stored incorrectly.
Temperature abuse during storage can cause the medication to become unsafe. This means the drug might not work correctly or could cause harm if the temperature was not properly controlled.
Prescription patients with Verapamil HCL ampules (2.5 mg/ML, 2ML, 5/pack) from Pfizer. Those who received the product through McKesson Medical-Surgical may be affected.
Check for the product name 'Verapamil HCL ampules', strength 2.5 mg/ML, 2ML (5/pack), and manufacturer Pfizer. The recall covers products distributed by McKesson Medical-Surgical.
Verify the product name, strength, and packaging to confirm if it matches the recalled items.
The recall indicates potential temperature abuse risks, but the product may still be safe if stored correctly. Consult your healthcare provider for specific advice.
Check for the product name 'Verapamil HCL ampules', strength 2.5 mg/ML, 2ML (5/pack), and manufacturer Pfizer. The recall covers products distributed by McKesson Medical-Surgical.
The recall does not specify a remedy, so contact your healthcare provider or pharmacist for guidance on safe handling.
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-1100-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1100-2022 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.
