Bard Peripheral Vascular Inc - EQUISTREAM LongTerm Hemodialysis Catheter - Class 2 Recall
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product code:5905240, 14.5 Fr. Alphacurve Catheter with Standard Kit, 24cm length, BARD, UDI# 00801741013805 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - GLIDEPATH LongTerm Hemodialysis Catheter - Class 2 Recall
GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393270, 14.5F, Straight, 27cm length, BARD, UDI: 00801741012198 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - GLIDEPATH LongTerm Hemodialysis Catheter - Class 2 Recall
GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393230, 14.5F, Straight, 23cm length, BARD, UDI: 00801741012181 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - EQUISTREAM XK LongTerm Hemodialysis Catheter - Class 2 Recall
EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913190, 16F, Straight, 19cm length, BARD, UDI: 00801741013836 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - GLIDEPATH LongTerm Hemodialysis Catheter - Class 2 Recall
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397310, 14.5F, straight, 31cm length, BARD, UDI: 00801741012327 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - GLIDEPATH LongTerm Hemodialysis Catheter - Class 2 Recall
GlidePath Long-Term Hemodialysis Catheter, REF/Product code:5396190, 14.5F, Alphacurve, 19cm length, BARD, UDI: 00801741012242 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - EQUISTREAM XK LongTerm Hemodialysis Catheter - Class 2 Recall
EQUISTREAM XK Alphacurve Long-Term Hemodialysis Catheter REF/Product code:5915240, 16F, 24cm length, BARD, UDI: 00801741013904 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - GLIDEPATH LongTerm Hemodialysis Catheter - Class 2 Recall
GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393190, 14.5F, Straight, 19cm length, BARD, UDI: 00801741012174 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - EQUISTREAM LongTerm Hemodialysis Catheter - Class 2 Recall
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit, 19 cm length, BARD, UDI# 00801741013799 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Bard Peripheral Vascular Inc - EQUISTREAM LongTerm Hemodialysis Catheter - Class 2 Recall
EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5904270, 14.5F, Straight ,27cm length, BARD, UDI: 00801741013775 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 27, 2019 Category: Medical Devices Source Type: alerts

Medical Components, Inc dba MedComp - 14F SLX Double Lumen Full Tray - Class 2 Recall
14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423 Product Usage: An aid for introducing a hemodialysis catheter (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 9, 2019 Category: Medical Devices Source Type: alerts

Medical Components, Inc dba MedComp - 14F SLX Double Lumen Full Tray - Class 2 Recall
14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061425 Product Usage: An aid for introducing a hemodialysis catheter (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 9, 2019 Category: Medical Devices Source Type: alerts

Medical Components, Inc dba MedComp - 14F SLX Double Lumen Full Tray - Class 2 Recall
14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061424 Product Usage: An aid for introducing a hemodialysis catheter (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 9, 2019 Category: Medical Devices Source Type: alerts

Fresenius Medical Care Renal Therapies Group, LLC - Class 2 Recall
Liberty Cycler Cassettes (a disposable cassette that is intended to be used to perform peritoneal dialysis (APD) in conjunction with the Liberty cycler as follows: (1) LIBERTY Line Cycler Set with Stay-safe connectors (Dual Patient Connector) Part Number: 050-87212 (2) LIBERTY Line Cycler Set with Stay-safe connectors (Single Patient Connector) Part Number: 050-87215 (3) LIBERTY Integrated Cycler Set with single Stay-safe patient connector and extended drain line Part Number: 050-87216 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2019 Category: Medical Devices Source Type: alerts

COVIDIEN LLC - MAHURKAR and Argyle acute hemodialysis catheters - Class 2 Recall
MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009 8813793013 8813794005 8813794009 8813816005 8813816009 8813817005 8813817009 8815668007 8815668011 8815668021 8815668027 8817142005 8817143005 8817145005 8817146001 8817146007 8817149007 8817232018 8817232019 8817277007 8817277011 8817277021 8817277027 8830414001 8830414002 8830415001 8830415003 8830416001 8830416003 8830416021 8830416023 8831173010 8831173011 8831173012 8831661001 8831662001 8831663001 8831663002 8831663021 8831663022 8832539001 8832539002 8832539003 8832539006 8832539007 8888115132 8888115133 8888115162 8888115163 8888115192 88...
Source: Medical Device Recalls - July 10, 2019 Category: Medical Devices Source Type: alerts