Drug recall
O.R. SCISSORS, S/B, 5.5 STERILE, Medline Item No. DYND04000
FDA recall event 95843 · Class II · MEDLINE INDUSTRIES, LP - Northfield
Key facts
| Event ID | 95843 |
|---|---|
| Recall numbers | Z-0754-2025, Z-0755-2025, Z-0756-2025, Z-0757-2025, Z-0758-2025, Z-0759-2025, Z-0760-2025 |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield |
| Product type | Devices |
| Products | O.R. SCISSORS, S/B, 5.5 STERILE, Medline Item No. DYND04000, RUMMELL, Medline Item No. ST006ST, STERILE MAGILL FORCEP (MAGF9), Medline Item No. 66790, STERILE STRT KELLY HEMOSTAT (SK8039S), Medline Item No. 66695, ST IUD REMOVAL HOOK 10" (504090), Medline Item No. I68785 and 2 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. |
| Initiation date | Nov 12, 2024 |
| Report date | Jan 1, 2025 |
| City | Northfield |
| State | IL |
| Country | United States |
| FEI number | 1417592 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: