Drug recall
Medline Convenience Kits: 1) ADMIT KIT, Model Number: DYKA1343A
FDA recall event 98329 · Class II · Medline Industries, LP
Key facts
| Event ID | 98329 |
|---|---|
| Recall numbers | Z-1384-2026, Z-1385-2026, Z-1386-2026, Z-1387-2026, Z-1388-2026, Z-1389-2026, Z-1390-2026, Z-1391-2026, Z-1392-2026, Z-1393-2026, Z-1394-2026, Z-1395-2026 and 30 more |
| Recalling firm | Medline Industries, LP |
| Product type | Devices |
| Products | Medline Convenience Kits: 1) ADMIT KIT, Model Number: DYKA1343A, Medline Convenience Kits: 1) ANCILLARY PACK-LF, Model Number: DYNJ0185290G; 2) OPEN HEART ANESTHESIA ICC-A, Model Number: DYNJ905567A, Medline Convenience Kits: 1) ARTHROSCOPY CDS, Model Number: CDS984609B; 2) ARTHROSCOPY TRAYS, Model Number: DYNJ22501G; 3) ARTHROSCOPY PACK, Model Number: DYNJ32715F; 4) CHS ARTHROSCOPY PACK, Model…, Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS, Model Number: CDS982407N; 2) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431K; 3) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431O; 4) KIT…, Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT, Model Number: DYKE1455B; 2) GI LAB OTHER ENDO KIT, Model Number: DYKE1721 and 37 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however… |
| Initiation date | Jan 7, 2026 |
| Report date | Feb 25, 2026 |
| City | Northfield |
| State | IL |
| Country | United States |
| FEI number | 1417592 |
At a glance
- 10–99 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: