Recall
Medline medical procedure kits labeled as follows: a) GYN CDS, REF DYNJ905499B; b) GYN LAP, REF DYNJ909936; c) GYN LAPAROSCOPY, REF DYNJ902371J; d) GYN LAPAROSCOPY, REF DYNJ905509F; e) GYN LAPAROSCOPY II, REF DYNJS2030F; f) LAP ROBOTIC,…
MEDLINE INDUSTRIES, LP - Northfield · 22 March 2024
- Status
- Recall open, classified
- Why, in the FDA's words
- “A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.”
- Recall began
- 22 March 2024
- Company
- MEDLINE INDUSTRIES, LP - Northfield
- Device type
- Product code (OHD)
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.