FDA Device recall Z-2430-2026
Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M
- FDA Device
- Class II
- ongoing
- Published 2026-06-24
On 2026-06-24 the FDA classified a Class II recall of Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M by Medline Industries, citing kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2430-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-04-27 |
| Published | 2026-06-24 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M
Reason
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Identifiers
| code_info | UDI-DI 10198459028274 Lot 25LMI820 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2430-2026%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.