Drug recall
BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433
FDA recall event 90707 · Class II · CAREFUSION
Key facts
| Event ID | 90707 |
|---|---|
| Recall numbers | Z-1752-2022, Z-1753-2022, Z-1754-2022, Z-1755-2022, Z-1756-2022, Z-1757-2022, Z-1758-2022, Z-1759-2022, Z-1760-2022 |
| Recalling firm | CAREFUSION |
| Product type | Devices |
| Products | BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433, BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock, REF: MX4436, BD MaxGuard Extension Set, REF: ME1069, BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166, BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171 and 4 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be… |
| Initiation date | Aug 1, 2022 |
| Report date | Sep 28, 2022 |
| City | San Diego |
| State | CA |
| Country | United States |
| FEI number | 3012410077 |
At a glance
- 1–9 Products in this recall
- 1–9 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: