Becton Dickinson & Company Recall: PowerLoc MAX Power Injectable Infusion Port Access Kit;
Becton Dickinson & Company Recall: PowerLoc MAX Power Injectable Infusion Port Access Kit; is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Becton Dickinson & Company; Product: PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 00801741044151), 2131915
| Recalling firm | Becton Dickinson & Company |
|---|---|
| Product | PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 00801741044151), 2131915 (UDI 00801741044168), 2131975 (UDI 00801741044175), 2132010 (UDI 00801741044151), 2132015 (UDI 00801741044199), 2132075 (UDI 00801741044205), 2132210 (UDI 00801741044212), 2132275 (UDI 00801741044236), 2141910 (UDI 00801741044243), 2141915 (UDI 00801741044250), 2141975 (UDI 00801741044267), 2142010 (UDI 00801741044274), 2142015 (UDI 00801741044281), 2142075 (UDI 00801741044298), 2142210 (UDI 00801741044304), 2142215 (UDI 00801741044311), 2142275 (UDI 00801741044328) |
| Reason for recall | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution |
| Recall initiated | 20200619 |
| Recall number | Z-2662-2020 |
| Category | device |
| State | NJ |
| Country | United States |
$29/mo
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