Cardinal Health is recalling Presource Kits with catalog numbers PE23NSMEA, PE23NSMEC, PE23SENLA, PE23SENLC, PE30EAGT6-9, PE30EAGTB, PE35NSB10-19, PE35NSBL1-19, PE3ESKSG1-2, PE3ESKSGA, PECGNAAU4-7, PEDHSPNH3, PEDHSPNHE, PEHDMJVCG, PEMHETMHA, PEMHNFMH1-2, PEMHNSB10-11, PEMHNSBH4-9, PEMHNSBHP, PEMHNSBHQ, PEMHNSBHR, PEV2CL011-106, PEV2FSNYA, PEV2FSNYB, PEV2OT10F, PEV2OT10G, PEV2OT10H, PEV2OT10I, PEX4SSMNA, PG35NSBL1, PG35NSBLA, PNVMESCH8, PNVMESCH9, PQMHETMHP due to potential endotoxin contamination in non-sterile surgical strips and patties. Consumers should stop using these kits immediately.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Cardinal Health is recalling several Presource Kits that may contain endotoxin contamination in non-sterile surgical strips and patties. This could pose a risk of infection or other health issues if used improperly. Affected kits have specific catalog numbers and lot numbers listed in the recall notice.
Endotoxins are bacterial components that can cause infections when introduced into the body. Non-sterile surgical strips and patties in these kits may contain endotoxins, which could lead to infections or adverse reactions if used during medical procedures.
Patients and medical professionals who own or use the recalled Presource Kits for nasal, ear, sinus, septoplasty, or other surgical procedures are most at risk. The specific kits affected include those with catalog numbers listed in the recall notice.
Check the catalog number on the kit packaging. Affected kits include PE23NSMEA, PE23NSMEC, PE23SENLA, PE23SENLC, PE30EAGT6-9, PE30EAGTB, PE35NSB10-19, PE35NSBL1-19, PE3ESKSG1-2, PE3ESKSGA, PECGNAAU4-7, PEDHSPNH3, PEDHSPNHE, PEHDMJVCG, PEMHETMHA, PEMHNFMH1-2, PEMHNSB10-11, PEMHNSBH4-9, PEMHNSBHP, PEMHNSBHQ, PEMHNSBHR, PEV2CL011-106, PEV2FSNYA, PEV2FSNYB, PEV2OT10F, PEV2OT10G, PEV2OT10H, PEV2OT10I, PEX4SSMNA, PG35NSBL1, PG35NSBLA, PNVMESCH8, PNVMESCH9, and PQMHETMHP. Also check the lot number listed in the recall notice.
The recalled Presource Kits may contain endotoxins that could cause infections if used during medical procedures.
Endotoxins are bacterial components that can cause infections when introduced into the body. The recall indicates that non-sterile surgical strips and patties in these kits may contain endotoxins.
Check the catalog number on the kit packaging. Affected kits include specific catalog numbers listed in the recall notice, such as PE23NSMEA, PE23NSMEC, PE23SENLA, and others.
The recall does not specify a return process, but you should stop using the kit immediately and contact Cardinal Health for further instructions.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0913-2025 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0913-2025 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.
