Cardinal Health recalls robotic hysterectomy Presource Kits (PB4FRHWFA, PB4FRHWFB, PB4FRHWFC) due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits may pose infection risks during surgery.
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Cardinal Health is recalling robotic hysterectomy Presource Kits that could contain endotoxins in non-sterile surgical strips and patties. This contamination risk could lead to infections during surgery if the kits are used without proper sterilization.
The kits contain non-sterile surgical strips and patties that may have endotoxins. Endotoxins are bacterial components that can cause infections if introduced into the body during surgery.
Surgical teams using the recalled Presource Kits for robotic hysterectomies are most at risk. Patients undergoing these procedures with the affected kits could face infection risks.
Check for the catalog numbers PB4FRHWFA, PB4FRHWFB, or PB4FRHWFC on the kit packaging. The lot numbers listed (e.g., 6701856, 7331357) indicate specific batches to avoid.
Verify the catalog number and lot number on the Presource Kit packaging to confirm if it is affected.
The kits may contain endotoxins in non-sterile surgical strips and patties, which could lead to infections during surgery.
The affected catalog numbers are PB4FRHWFA, PB4FRHWFB, and PB4FRHWFC.
Check the catalog number on the packaging and compare it to PB4FRHWFA, PB4FRHWFB, or PB4FRHWFC. Also, verify the lot number (e.g., 6701856, 7331357).
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1133-2025 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1133-2025 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.
