Bard recalls EQUISTREAM long-term hemodialysis catheters with preloaded styet (model 5903190) due to tunneler tip breaking during placement, potentially causing complications. Affected units include specific lot numbers from August 2020.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Bard is recalling certain long-term hemodialysis catheters because the tunneler tip may break during catheter placement. This could lead to complications for patients needing dialysis treatment.
The molded tip of the tunneler can break during catheter placement. This breakage might cause the catheter to malfunction or dislodge, leading to complications like infection or bleeding.
Patients using hemodialysis treatments with the recalled catheters are most at risk. Healthcare providers who place these catheters may also be affected.
Check for the model number 5903190 on the catheter packaging. The catheter has a 14.5F size, straight configuration, and 19cm length. Affected units were sold with specific lot numbers from July to August 2020.
Inspect the tunneler tip for cracks or damage before use. If broken, stop using the catheter immediately.
Reach out to your healthcare provider to discuss alternative catheter options if the tunneler tip is damaged.
The recall is due to complaints about the tunneler tip breaking during catheter placement, which could cause complications.
Check for model number 5903190, 14.5F size, straight configuration, and 19cm length. Affected units were sold with specific lot numbers from July to August 2020.
Stop using the catheter immediately and contact your healthcare provider for alternative options.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2371-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2371-2019 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.
