Recall Z-3061-2026
- Recall number
- Z-3061-2026
- Event number
- 99334
- Firm
- Medline Industries, LP
- Firm FEI
- 1417592
- Product code
- OJK
- Status
- Open, Classified
- Initiated
- 2026-06-12
- Posted
- 2026-08-31
- Root cause
- Nonconforming Material/Component
Product#
Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A; 3) CATARACT PREOP KIT, Model Number: DYKS1583A; 4) CATARACT PREOP KIT, Model Number: DYKS1583B
Reason for Recall#
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is compromised, patients and users may be exposed to microbial contamination. Potential health consequences may include no injury, localized infection, or, less commonly, more serious infection requiring medical treatment, antimicrobial therapy, procedural intervention, or hospitalization. In rare cases, particularly in critically ill or immunocompromised patients, severe infection could become life-threatening.