FDA Device recall Z-2790-2026
Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P
- FDA Device
- Class II
- ongoing
- Published 2026-07-29
On 2026-07-29 the FDA classified a Class II recall of Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P by Medline Industries, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2790-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-11 |
| Published | 2026-07-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medline Industries |
| Distribution | CT, FL, KS, MA, MD, MT, NY, OH, OR, VA |
Product
Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P
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.
Identifiers
| code_info | UDI/DI 10198459098109 (each) 40198459098100 (case), Lot Numbers: 25AMJ225, 25CMF838, 24KME164, 25DMB248, 25FMD941, 25GMB662, 25GMG296. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2790-2026%22
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