Recall
Medline convenience kits labeled as: 1) MAJOR GYN PACK, Medline Kit SKU DYNJG001030C; 2) GYN LITHOTOMY PACK, Medline Kit SKU DYNJT8166; 3) OPEN HEART PACK, Medline Kit SKU DYNJ47638B; 4) EAST DAVINCI, Medline Kit SKU DYNJ900949C; 5)…
Medline Industries, LP · 10 July 2026
- Status
- Recall open, classified
- Why, in the FDA's words
- “Kits contain a potentially contaminated component which were recalled by the manufacturer”
- Recall began
- 10 July 2026
- Company
- Medline Industries, LP
- Device type
- Product code (LRO)
- Concerns
- K213481
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.