FDA recall Z-0510-2026
Medline Industries, LP · Class II · device
Product
MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.
Reason for recall
Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
Distribution
US: MO
Key facts
- Status
- Ongoing
- Initiation date
- 2025-10-03
- Report date
- 2025-11-26
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Northfield, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0510-2026