Bard recalls EQUISTREAM XK Long-Term Hemodialysis Catheters with incorrect peel-apart introducer sheath. This may cause complications during dialysis procedures. Affected units have specific lot numbers and model details.
Incorrect Peel-Apart Introducer Sheath in Kit.
Bard is recalling EQUISTREAM XK Long-Term Hemodialysis Catheters that have an incorrect peel-apart introducer sheath in the kit. This could lead to complications during dialysis treatments if the catheter is used without proper sheath alignment.
The incorrect peel-apart introducer sheath may not align properly with the catheter during insertion. This could cause complications such as blockages or infections during dialysis treatments if the sheath is not correctly positioned.
Hemodialysis patients using the EQUISTREAM XK catheter with the specific lot number RECV3572 are affected. Patients using this model for long-term dialysis are at risk if the sheath is not correctly aligned.
Check for the model 'EQUISTREAM XK Long-Term Hemodialysis Catheter' with lot number RECV3572 and the specific reference code 5913230/:(01)00801741013843. The catheter has a 16F size.
Verify the lot number and reference code on the catheter packaging to confirm if it matches RECV3572 and 5913230/:(01)00801741013843.
No, only catheters with lot number RECV3572 and reference code 5913230/:(01)00801741013843 are affected.
Check the lot number and reference code on your catheter packaging. If it matches the affected details, contact Bard for further instructions.
The recall indicates a potential risk, so it's recommended to check if your catheter is affected before continuing use.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2208-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-2208-2020 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.
