Medline recalls specific pediatric heart Moses kits with BD PurPrep 26mL that may have low levels of Bacillus species. Affected kits include models DYNJ910103B and DYNJ910961A with certain lot numbers.
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
Medline is recalling pediatric heart Moses kits and basic heart CDS kits that contain BD PurPrep 26mL. These kits may be contaminated with low levels of Bacillus species, which could pose a health risk if used improperly.
The kits contain BD PurPrep 26mL which may have low levels of Bacillus species. Bacillus species are bacteria that can cause infections, especially in medical settings where sterile procedures are critical.
Healthcare workers using Medline pediatric heart Moses kits or basic heart CDS kits with specific lot numbers are most at risk. Patients receiving these kits could be affected if the contamination leads to infection.
Check for Medline kits labeled as 'KIT PEDIATRIC OPEN HEART MOSES' (SKU DYNJ910103B) or 'BASIC HEART CDS' (SKU DYNJ910961A). Look for lot numbers 25FBR237, 25ABM761, 25BBD107, 25FBD534, or 25FBL772.
Look for the specific product labels and lot numbers listed in the recall notice to confirm if your kit is affected.
The kits may contain low levels of Bacillus species in BD PurPrep 26mL, which could lead to infections if used improperly.
Affected kits include KIT PEDIATRIC OPEN HEART MOSES (SKU DYNJ910103B) and BASIC HEART CDS (SKU DYNJ910961A) with lot numbers 25FBR237, 25ABM761, 25BBD107, 25FBD534, or 25FBL772.
The recall states the kits may be contaminated, but the remedy is not specified. Check the labels to confirm if your kit is affected before taking action.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2788-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2788-2026 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.
