FDA Device recall Z-3210-2026
Convenience kits CATARACT PACK DYNJ59881A
- FDA Device
- Class II
- ongoing
- Published 2026-09-23
On 2026-09-23 the FDA classified a Class II recall of Convenience kits CATARACT PACK DYNJ59881A by Medline Industries, citing kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3210-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-31 |
| Published | 2026-09-23 |
| Last updated | 2026-09-29 05:30 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Convenience kits CATARACT PACK DYNJ59881A
Reason
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
Identifiers
| code_info | UDI-DI 10198459020612 Lot 25GBP246 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-29 05:30 UTC. Current status: ongoing.
Other recalls by Medline Industries
- Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
FDA Device · Class I · 2026-10-07 · Medline Industries - Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants: MDR510094 PENDANT F/ MDR107002E MDR520094 PENDANT F/…
FDA Device · Class I · 2026-10-07 · Medline Industries - Medline convenience kits containing Healthmark Instrument Channel Brushes
FDA Device · Class II · 2026-09-30 · Medline Industries - Medline Convenience Kits: 1) MAJOR NEURO VCH, Catalog Number: DYNJ39218I
FDA Device · Class II · 2026-09-30 · Medline Industries - Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197
FDA Device · Class II · 2026-09-30 · Medline Industries
All Medline Industries recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3210-2026%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.