Z-2790-2026 Class II Ongoing
FDA device recall Z-2790-2026 was initiated by Medline Industries, LP on June 11, 2026 and is designated Class II. Reason for recall: 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. The recall status is ongoing. Affected quantity: 574 kits.
Recall Details
- Product Type
- Devices
- Report Date
- July 29, 2026
- Initiation Date
- June 11, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 574 kits
Product Description
Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P
Reason for Recall
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.
Distribution Pattern
US: CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.
Code Information
UDI/DI 10198459098109 (each) 40198459098100 (case), Lot Numbers: 25AMJ225, 25CMF838, 24KME164, 25DMB248, 25FMD941, 25GMB662, 25GMG296.