Mckesson Medical-Surgical recalls paracentesis trays due to temperature abuse during manufacturing. This may affect prescription products containing lidocaine hydrochloride. No specific remedy is stated in the recall notice.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical has recalled paracentesis/thoracentesis trays that contain lidocaine hydrochloride. The recall is due to temperature abuse during manufacturing, which could lead to unsafe conditions for patients.
The recall mentions 'cGMP deviations: Temperature abuse' which means the product was exposed to unsafe temperatures during manufacturing. This could compromise the safety and effectiveness of the lidocaine hydrochloride solution.
Prescription patients who received the recalled paracentesis trays from Mckesson Medical-Surgical. Healthcare providers using these trays for medical procedures may be at risk.
The recalled product is a paracentesis/thoracentesis tray (10 units per case) containing lidocaine hydrochloride 1% (5mL) for prescription use. It was manufactured by Becton Dickinson and distributed by Mckesson Medical-Surgical.
Look for the product name and manufacturer information on the tray to confirm if it matches the recalled items.
The recall is due to cGMP deviations related to temperature abuse during manufacturing.
The recall notice does not specify a remedy or action for affected customers.
The recall notice states that Mckesson Medical-Surgical cannot identify the particular lot number for each consignee.
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-1122-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1122-2022 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.
