FDA Device recall Z-2711-2024
Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A
- FDA Device
- Class II
- ongoing
- Published 2024-08-28
On 2024-08-28 the FDA classified a Class II recall of Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A by Medline Industries Northfield, citing A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2711-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-22 |
| Published | 2024-08-28 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ908566
Reason
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Identifiers
| code_info | a) REF DYNJ909171A, UDI/DI 40195327384570 (case), 10195327384579 (unit), Lot Numbers: 23ELA235, 23ELA709, 23FLA843, 23F…a) REF DYNJ909171A, UDI/DI 40195327384570 (case), 10195327384579 (unit), Lot Numbers: 23ELA235, 23ELA709, 23FLA843, 23FLB029, 23ILA269, 23JLA515, 23KLA152; b) REF DYNJ905510D, UDI/DI 40193489967495 (case), 10193489967494 (unit), Lot Numbers: 22FMD495, 22FME413, 22JMG896, 23CMA506, 23DMF104, 23DMG416, 23DMH216, 23FMB741, 23GMI014, 23LMC545; c) REF DYNJ902388L, UDI/DI 40195327505876 (case), 10195327505875 (unit), Lot Numbers: 23KBP772; d) REF DYNJ908566, UDI/DI 40195327086450 (case), 10195327086459 (unit), Lot Numbers: DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566, DYNJ908566 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2711-2024%22
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