Bard recalls EQUISTREAM long-term hemodialysis catheters with preloaded styet (model 5903270) due to molded tip breaking during catheter placement, potentially causing complications.
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 specific hemodialysis catheters that may have a broken molded tip during placement. This could lead to complications if the catheter becomes dislodged or damaged.
The molded tip of the tunneler can break during catheter placement, which may cause the catheter to become dislodged or damaged. This could lead to complications such as infection or bleeding if the catheter is no longer properly secured.
Hemodialysis patients using the recalled catheters (model 5903270, 14.5F, straight, 27cm) are most at risk. Healthcare providers who placed these catheters should check for tip damage.
Check for the model number 5903270, 14.5F, straight, 27cm length on the catheter. The recall includes catheters with lot number RECW0913 expiring 3/31/2020.
Inspect the catheter for any signs of a broken or damaged molded tip, especially at the end where the tunneler connects.
If you have the recalled catheter, contact your healthcare provider to determine if the tip is damaged and whether replacement is needed.
Bard is recalling these catheters due to complaints about the molded tip breaking during placement, which could cause complications.
Look for the model number 5903270, 14.5F, straight, 27cm length, and lot number RECW0913 expiring 3/31/2020.
No, but you should check for tip damage and contact your healthcare provider if you suspect the tip is broken.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2373-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2373-2019 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.
