Recall- Non-functioning intraosseous access & needlestick injuries

Company: Becton, Dickinson and Company

Date of Enforcement Report: 6/22/2022

Product:

Intraosseous Needle Set Kits, Intraosseous Manual Driver Kits, Intraosseous Powered Drivers

Reason:

Product issues may result in delays in care due to limited or non-functioning intraosseous access or could also lead to needlestick injuries

Recalling Firm/Manufactuer:

BD (Becton, Dickinson and Company) on 6/22/2022. Voluntary: Firm initiated

Volume of product in Commerce:

See full list of impacted products and lot numbers here:

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-announces-voluntary-recall-intraosseous-products

About the author

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

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