Medline recalls Basic Nerve Block Trays with model PAIN0150C due to potential sterility issues from calibration problems during sterilization. Affected kits may not be sterile, risking infection.
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Medline is recalling Basic Nerve Block Trays with model number PAIN0150C because calibration issues during sterilization could compromise sterility. This means the kits might not be sterile, increasing infection risk for medical users.
The calibration issues during sterilization might lead to the kits not being properly sterilized. This could result in the kits not meeting sterility standards, potentially causing infections during medical procedures.
Healthcare professionals using these kits for nerve block procedures are most at risk. Patients receiving procedures with these kits could face infection if the kits are not sterile.
Check for model number PAIN0150C on the kit. These kits were sold with lot numbers starting with 21JBV886 and were distributed in 2021.
Verify if the kit has been sterilized using the validated process by checking the lot number and model.
Medline identified calibration issues during sterilization that could impact the sterility assurance level of the kits.
The model number is PAIN0150C.
Look for model number PAIN0150C and lot numbers starting with 21JBV886.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2116-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2116-2026 from Medline. 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.
