FDA Device recall Z-2429-2026
Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F
- FDA Device
- Class II
- ongoing
- Published 2026-06-24
On 2026-06-24 the FDA classified a Class II recall of Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F 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-2429-2026 |
| 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: (82)LABOR & DELIVERY C-SECTION DYNJ907895F
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 10198459366390 Lot 25KBL873 |
|---|
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-2429-2026%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.