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Bard Access Systems Recall: 16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted S

Bard Access Systems Recall: 16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted S is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Bard Access Systems; Product: 16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an AirGuard introducer. The devi

Recalling firmBard Access Systems
Product16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an AirGuard introducer. The device is used for patients requiring hemodialysis. The HemoStar XK catheter is made of radio-opaque polyurethane and allows for flow rates as high as 500 ml/min during hemodialysis treatment.
Reason for recallBard Access Systems is recalling one lot of 16 Fr HemoStar XK Long Term Hemodialysis Catheters because they were identified with an incorrect expiration date, 03/2015 rather than 10/2013.
ClassificationClass III (least serious — unlikely to cause adverse health consequences)
StatusTerminated
DistributionNational US distribution only: MO, KS, AZ, OK, OR, AL, MA, TX, FL, MI, OH, LA, NJ, NC, WA, AR.
Recall initiated20120807
Recall numberZ-2277-2012
Categorydevice
StateUT
CountryUnited States

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