Recall
MEDLINE medical convenience kits labeled as: 1) LAPAROTOMY GYN CDS, Medline Kit Number/SKU CDS983529O; 2) GYN ROBOTIC PK-LF, Medline Kit Number/SKU DYNJ52432M; 3) TAH PACK, Medline Kit Number/SKU DYNJ60646A; 4) TUBAL LIGATION RFD,…
Medline Industries, LP · 9 Sept 2026
- Status
- Recall open, classified
- Why, in the FDA's words
- “Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.”
- Recall began
- 9 Sept 2026
- Company
- Medline Industries, LP
- Device type
- Product code (PUI)
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.