Mckesson Medical-Surgical recalls Epidural Tray products due to temperature abuse risks. Affected items may have been shipped with improper temperature control.
cGMP deviations: Temperature abuse
Mck: Mckesson Medical-Surgical has recalled certain Epidural Trays for nerve block procedures due to temperature abuse risks. This could lead to unsafe medical conditions if the products were exposed to incorrect temperatures during storage or transport.
The recall is for temperature abuse, meaning the products may have been exposed to incorrect temperatures during storage or transport. This could lead to unsafe medical conditions if the products were not maintained at proper temperature conditions.
Healthcare providers who received the recalled Epidural Trays for nerve block procedures are likely affected. Patients receiving these products under a prescription may be at risk if the products were improperly stored.
Check for the product name 'Epidural Tray, Nerve Block Single shot, Rx only' with lot number #182207. The recall covers items distributed by Mckesson Medical-Surgical that may have been shipped with improper temperature control.
Identify the product name and lot number to confirm if it's affected.
The recall is due to temperature abuse risks, meaning the products may have been exposed to incorrect temperatures during storage or transport.
The official notice does not specify a remedy for this recall, so check with Mckesson Medical-Surgical for further instructions.
Check for the product name 'Epidural Tray, Nerve Block Single shot, Rx only' with lot number #182207.
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-1010-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1010-2022 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.
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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.
