CLASS II · ModerateFDA

Medline Industries, LP recalls Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES

📅 Jun 11, 2026 · 📍 CT, FL, KS, MA, MD, MT, NY, OH +2

Recalling company: Medline Industries, LP
Product: Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES, Medline Kit SKU DYNJ910103B; 2) BASIC HEART CDS, Medline Kit SKU DYNJ910961A.
Reason: 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.
Classification: Class II – may cause temporary or medically reversible health consequences
Recall date: Jun 11, 2026
Reported: Jul 29, 2026
Distribution: US: CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.
Status: Ongoing
Quantity: 155 kits
Lot / codes: Medline Kit SKU DYNJ910103B, UDI/DI 10198459346873 (each) 40198459346874 (case), Lot Number 25FBR237; Medline Kit SKU DYNJ910961A, UDI/DI 10198459213342 (each) 40198459213343 (case), Lot Number 25ABM761; Medline Kit SKU DYNJ910961A, UDI/DI 10198459213342 (each) 40198459213343 (case), Lot Number 25BBD107; Medline Kit SKU DYNJ910961A, UDI/DI 10198459213342 (each) 40198459213343 (case), Lot Number 25FBD534; Medline Kit SKU DYNJ910961A, UDI/DI 10198459213342 (each) 40198459213343 (case), Lot Number 25FBL772.
Company location: Northfield, IL
Recall type: Voluntary: Firm initiated
Recall number: Z-2788-2026
Agency: U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2788-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.