Smiths Medical recalls portex devices with missing sterilization labeling that prohibits reuse. Affected units include specific lot numbers. Contact for remedy details.
The labeling was missing information on sterilization and prohibition of reuse.
Smiths Medical is recalling portex Loss of Resistance Devices with missing sterilization labeling information. This means the devices could be reused improperly, which is unsafe.
The devices lack proper labeling about sterilization requirements. This could allow improper reuse, which might lead to infections or other complications.
Healthcare professionals using these devices for medical procedures are most at risk. Patients receiving treatments with the recalled devices may be affected.
Check for lot numbers 3980977, 3986734, 3994302, 3994303, or 4001003 on the device packaging. The product is a Smiths Medical portex Loss of Resistance Device.
Look for lot numbers 3980977, 3986734, 3994302, 3994303, or 4001003 on the device packaging.
The labeling was missing information on sterilization and prohibition of reuse.
Check the lot number to see if it's affected. If so, contact Smiths Medical for further instructions.
The recall is due to missing labeling that could allow improper reuse, but no specific injury risk is stated.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0152-2022 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0152-2022 from Smiths Medical. 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.
