Cardinal Health recalls Presource Kits with NEWNAN SMR PACK (Catalog SEN21SPPMB) due to unexpected endotoxin variability in Neurological Sponges. Affected lots from 2019-2020 may pose risks.
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Cardinal Health is recalling Presource Kits containing NEWNAN SMR PACK sponges because they have unexpected endotoxin level variations. This could lead to infections or other health issues if used in medical procedures.
The sponges contain unexpected endotoxin levels that could cause infections or other health issues during medical procedures. Endotoxins are natural components of bacterial cell walls that can trigger immune responses.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving procedures with these kits may be affected if the sponges cause infections.
Check for the catalog number SEN21SPPMB on the kit. Affected lots include 15192 and 15463-1 from 2019-2020. The kits are sold under Cardinal Health Presource Kits.
Look for catalog number SEN21SPPMB and lot numbers 15192 or 15463-1 on the kit packaging.
The sponges have unexpected variability in endotoxin levels, which could lead to infections or other health issues during medical procedures.
Check the catalog number and lot numbers on the kit. If it matches the recalled items, contact Cardinal Health for instructions.
The recall is due to potential infection risks from endotoxin variability, but the remedy is not specified in the record.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2944-2026 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2944-2026 from Cardinal Health. 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.
