Bard recalls specific POWERPORT CLEARVUE catheter and NAUTILUS DELTA kit models that may cause loss of ECG signal during port placement procedures. Affected units include certain product codes and lot numbers.
Certain NAUTILUS DELTA Port Kit product code / lot number combinations may be at risk of experiencing a lack of or a loss of the intravascular ECG signal during port placement procedures when used in combination with the NAUTILUS DELTA" TCS.
Bard is recalling specific POWERPORT CLEARVUE catheter and NAUTILUS DELTA kit models that may cause loss of ECG signal during port placement procedures. This could lead to complications if the signal is lost during critical medical procedures.
The recalled product combinations may cause a lack or loss of intravascular ECG signal during port placement procedures when used with the NAUTILUS DELTA TCS. This could potentially lead to complications if the signal is lost during critical medical procedures.
Healthcare professionals using these specific catheter and kit models for vascular access procedures. Patients receiving these devices are at risk if the ECG signal is lost during port placement.
Check for product codes REBR1147, REBR1148, REBR1149, REBT0471, RECQ2162, or REBR1150 on the packaging or documentation. The affected products include POWERPORT CLEARVUE isp and Slim catheters with specific sizes and the Intermediate NAUTILUS DELTA Kit.
Identify if your kit includes product codes REBR1147, REBR1148, REBR1149, REBT0471, RECQ2162, or REBR1150.
Certain combinations of the POWERPORT CLEARVUE catheter and NAUTILUS DELTA kit may cause loss of intravascular ECG signal during port placement procedures when used with the NAUTILUS DELTA TCS.
Check the product codes on your packaging to see if they are affected. If you have an affected product, contact Bard for further instructions.
The recall is for potential signal loss during procedures, but the hazard does not cause immediate injury or death in normal use.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2080-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2080-2019 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
