FDA Device recall Z-0361-2022
Venous Access Pack-LF Convenience Kit
- FDA Device
- Class II
- terminated
- Published 2021-12-22
On 2021-12-22 the FDA classified a Class II recall of Venous Access Pack-LF Convenience Kit by Medline Industries, citing naCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after 04/2020.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0361-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-10-27 |
| Published | 2021-12-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Venous Access Pack-LF Convenience Kit
Reason
NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after 04/2020.
Identifiers
| code_info | Model #: DYNJ36725B Lot #: 19UBB149 UDI: GTIN (01)40889942389163 EXP (17)2021-07-31 LOT (10)19UBB149 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0361-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.