Bard Peripheral Vascular Inc Recall: GlidePath Long-Term Hemodialysis Catheter with Preloa
Bard Peripheral Vascular Inc Recall: GlidePath Long-Term Hemodialysis Catheter with Preloa is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Bard Peripheral Vascular Inc; Product: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397310, 14.5F, straight,
| Recalling firm | Bard Peripheral Vascular Inc |
|---|---|
| Product | GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397310, 14.5F, straight, 31cm length, BARD, UDI: 00801741012327 |
| Reason for recall | 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. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA,MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI, WV, WY OUS: Australia, Canada, |
| Recall initiated | 20190531 |
| Recall number | Z-2393-2019 |
| Category | device |
| State | AZ |
| Country | United States |
$29/mo
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