FDA Medical devices recall ·
Medline medical convenience kits labeled as: NEURO PACK… recall
- Recall number
- Z-2790-2026
- Date
- (initiated June 11, 2026)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 574 kits
- Hazard tags
- Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI/DI 10198459098109 (each) 40198459098100 (case), Lot Numbers: 25AMJ225, 25CMF838, 24KME164, 25DMB248, 25FMD941, 25GMB662, 25GMG296.
Distribution
US: CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.
States: Connecticut Florida Kansas Massachusetts Maryland Montana New York Ohio Oregon Virginia
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2790-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.