Cardinal Health Inc. Recall: LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Pr
Cardinal Health Inc. Recall: LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Pr is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Cardinal Health Inc.; Product: LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottl
| Recalling firm | Cardinal Health Inc. |
|---|---|
| Product | LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle, Sterile, Distributed By Cardinal Health, Dublin, Ohio 43017, Made in India NDC: 70000-0088-1 |
| Reason for recall | Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility. |
| Classification | Class I (most serious — reasonable probability of serious health consequences or death) |
| Status | Ongoing |
| Distribution | Nationwide in the USA |
| Recall initiated | 20231031 |
| Recall number | D-0135-2024 |
| Category | drug |
| State | OH |
| Country | United States |
$29/mo
Try RecallGuard →