Medline medical procedure kits — Class II medical device recall Z-1918-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-06-05, distributed nationwide. Trumpet Needle Guide ring can detach when excessive pressure is applied.
| Recall number | Z-1918-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-03-01 |
| Classified | 2024-05-29 |
| Reported by FDA | 2024-06-05 |
| Distributed | Nationwide (US) |
| Quantity | 12,994 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 10195327330712, 10195327338619, 10195327424046, 40195327330713, 40195327338610, 40195327424047 |
| Lot numbers | 23JBX245, 23JBX367, 23JBX368, 23JBX369, 23JBX370, 23KBI682, 23KBT359, 23KBX629, 23LBA896, 23LBH751, 23LBL612, 23LBN930, 23LBV325, 23LBV326 |
| Model numbers | DYNDH1832, DYNJRA2210, DYNJRA9046, DYNJRA9046H |
Product
Medline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PUDENDAL KIT, REF DYNJRA2210; c) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046; d) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046H; Medical procedure convenience tray
Reason for recall
Trumpet Needle Guide ring can detach when excessive pressure is applied.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1918-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.