Class II
Medical Device Recall: MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.
Medline Industries, LP · October 3, 2025
Reason for Recall
Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
Distribution
US: MO
States Affected
MO
Quantity Affected
1024 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0510-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.