Baxter Healthcare Corporation Recall: Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H
Baxter Healthcare Corporation Recall: Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Baxter Healthcare Corporation; Product: Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H938176, for use in a pharmaceutical compounding device;
| Recalling firm | Baxter Healthcare Corporation |
|---|---|
| Product | Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H938176, for use in a pharmaceutical compounding device |
| Reason for recall | Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the ExactaMix and ExactaMix Pro compounders. Particulate matter has been observed within the inlet primary packaging inlet components, including within the sterile fluid path tubing, before use. |
| Classification | Class I (most serious — reasonable probability of serious health consequences or death) |
| Status | Ongoing |
| Distribution | Worldwide distribution. |
| Recall initiated | 20240820 |
| Recall number | Z-3085-2024 |
| Category | device |
| State | IL |
| Country | United States |
$29/mo
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