FDA Device recall Z-1595-2025
Medline Convenience kits used for various procedures: 1) DENTAL PACK-LF, Model Number: DYNJ84880
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Medline Convenience kits used for various procedures: 1) DENTAL PACK-LF, Model Number: DYNJ84880 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-1595-2025 |
| 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
Medline Convenience kits used for various procedures: 1) DENTAL PACK-LF, Model Number: DYNJ84880; 2) DENTAL PACK, Model Number: DYNJ56229A; 3) DENTAL PACK-LF, Model Number: PHS807626F; 4) DENTAL PACK SMGH, Model Number: DYNJ41929D; 5) DENTAL PACK, Model Number: DYNJ51841C; 6) NYGH-MINOR DENTAL-PLASTIC-LF, Model Number: DYNJ905551C
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) DYNJ84880, UDI-DI: 10195327432140(each), 40195327432141(case), Lot Number: 24JBL926; 2) DYNJ56229A, UDI-DI: 10198459…1) DYNJ84880, UDI-DI: 10195327432140(each), 40195327432141(case), Lot Number: 24JBL926; 2) DYNJ56229A, UDI-DI: 10198459108105(each), 40198459108106(case), Lot Number: 24JBV124; 3) PHS807626F, UDI-DI: 10198459028045(each), 40198459028046(case), Lot Number: 24JBV611; 4) DYNJ41929D, UDI-DI: 10198459160585(each), 40198459160586(case), Lot Number: 24JBW877; 5) DYNJ51841C, UDI-DI: 10195327522186(each), 40195327522187(case), Lot Number: 24KBA623; 6) DYNJ905551C, UDI-DI: 10195327556099(each), 40195327556090(case), Lot Number: 24KBN091 |
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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-1595-2025%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.