Bard Peripheral Vascular Inc EQUISTREAM XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EQUISTREAM XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Brand
Bard Peripheral Vascular Inc
Lot Codes / Batch Numbers
LOT RECV3572
Products Sold
LOT RECV3572
Bard Peripheral Vascular Inc is recalling EQUISTREAM XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F due to Incorrect Peel-Apart Introducer Sheath in Kit.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect Peel-Apart Introducer Sheath in Kit.
Recommended Action
Per FDA guidance
On 06/14/2019, an URGENT MEDICAL DEVICE RECALL NOTIFICATION letter was sent to each of the US consignees via FedEx with proof of delivery notification.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, FL, GA, ID, IL, IA, KY, LA, MD, MN, MT, NY, NC, OR, PA, TN, TX, VA, WA, WV, WI
Page updated: Jan 10, 2026