Becton Dickinson & Company recalls BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port…
May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i or UX-2000 Analyzers and lead to false elevations in RBC counts
Read the official notice →- Date
- 2022-03-02
- Country
- United States
- Brand
- Becton Dickinson &
- Product
- BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port…
- Classification
- Class III
- Units
- US Nationwide distribution in the state of IL.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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