FDA Device recall Z-1598-2025
Refer to RES
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Refer to RES by Medline Industries Northfield, citing there is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1598-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-03-03 |
| Published | 2025-04-23 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Refer to RES
Reason
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Identifiers
| code_info | 1) DYNJ84990, UDI-DI: 10195327444068(each), 40195327444069(case), Lot Number: 24IBE926; 2) DYNJ45711B, UDI-DI: 10193489…1) DYNJ84990, UDI-DI: 10195327444068(each), 40195327444069(case), Lot Number: 24IBE926; 2) DYNJ45711B, UDI-DI: 10193489856149(each), 40193489856140(case), Lot Number: 24IBE981; 3) DYNJ45266B, UDI-DI: 10193489852417(each), 40193489852418(case), Lot Number: 24IBF031; 4) DYNJ80737B, UDI-DI: 10198459050855(each), 40198459050856(case), Lot Number: 24IBF165; 5) DYNJ67785A, UDI-DI: 10193489945638(each), 40193489945639(case), Lot Number: 24IBG441; 6) DYNJ49675F, UDI-DI: 10198459113529(each), 40198459113520(case), Lot Number: 24IBG617; 7) DYNJ0579176B, UDI-DI: 10889942429844(each), 40889942429845(case), Lot Number: 24IBG732; 8) DYNJ23615D, UDI-DI: 10193489587012(each), 40193489587013(case), Lot Number: 24IBG752; 9) DYNJ44752D, UDI-DI: 10195327322342(each), 40195327322343(case), Lot Number: 24IBG844; 10) DYNJ83155, UDI-DI: 10195327236854(each), 40195327236855(case), Lot Number: 24IBH261; 11) DYNJ83423, UDI-DI: 10195327265410(each), 40195327265411(case), Lot Number: 24IBH595; 12) DYNJ64257C, UDI- |
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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-1598-2025%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.