Microvention, Inc. - Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System - Class 2 Recall
Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, and MV-AZ52030HD, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 14, 2020 Category: Medical Devices Source Type: alerts

Microvention, Inc. - Terumo AZUR Peripheral Coil System, Detachable 18 - Class 2 Recall
Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil Embolization System, REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45-480405, 45-480610, 45-480615, 45-480620, 45-480815, 45-480820, MV-AZ80520HL, MV-AZ80202HL, MV-AZ80204HL, MV-AZ80305HL, MV-AZ80310HL, MV-AZ80410HL, MV-AZ80420HL, MV-AZ80620HL, MV-AZ80820HL, and MV-AZ81020HL, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in C...
Source: Medical Device Recalls - February 14, 2020 Category: Medical Devices Source Type: alerts

Microvention, Inc. - Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil - Class 2 Recall
Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039, 45-750407, 45-750511, 45-750617, 45-750609, 45-750812, 45-750824, MV-AX50407CD, MV-AX50511CD, MV-AX50617CD, MV-AX50824CD, and MV-AX51019CD, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 14, 2020 Category: Medical Devices Source Type: alerts

Microvention, Inc. - Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil - Class 2 Recall
Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers 45-781032, 45-781238, 45-781434, 45-781639, 45-781836, 45-782040, 45-780202, 45-780204, 45-780304, 45-780308, 45-780413, 45-780516, 45-780620, 45-780724, 45-780828, 45-780928, MV-AX80202CL, MV-AX80204CL, MV-AX80304CL, MV-AX80308CL, MV-AX80413CL, MV-AX80516CL, MV-AX80620CL, MV-AX80724CL, MV-AX80828CL, MV-AX80928CL, MV-AX81032CL, MV-AX81238CL, MV-AX81434CL, MV-AX81639CL, and MV-AX82040CL, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 14, 2020 Category: Medical Devices Source Type: alerts

Microvention, Inc. - Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil - Class 2 Recall
Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers 45-651026 and 45-652050, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 14, 2020 Category: Medical Devices Source Type: alerts

Microvention, Inc. - Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil - Class 2 Recall
Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers 45-681026, 45-681434, 45-682050, and 45-680820, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 14, 2020 Category: Medical Devices Source Type: alerts

Stryker Endoscopy - PKG, BIPOLAR FORCEPS, MICRO TIP - Class 2 Recall
PKG, BIPOLAR FORCEPS, MICRO TIP, 45CM, P/N 0250080115 nationwide in US and worldwide: Algeria, Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, France, Germany, Greece, Guam, Guatemala, India, Italy, Japan, Jordan, Kuwait, Latin America, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Saudi Arabia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, Venezuela (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 13, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA Manufactured in Costa Rica. The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 150 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straight Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straight Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA; Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 260 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 150 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile.Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Nitinol Devices and Components, Inc. - HydroFinity Guidewire - Class 1 Recall
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2014 Category: Medical Equipment Source Type: alerts

Hospira Inc. - LifeShield LatexFree HEMA YType Blood Set IV Administration Set - Class 2 Recall
*** 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET, Nonvented, 88 Inch with 210 Micron Filter Pump, Prepierced Injection Site and Secure Lock; Made in Costa Rica; Product Inquiries should be directed to Hospira, Inc., Lake Forest, IL 60045 USA; *** 2) List Number 127200465 labeled in part: 12720-65 LifeShield LATEX-FREE HEMA; BLOOD SET, Nonvented, 81 Inch with 170 Micron Filter, Pump, Prepierced Injection Site and Secure Lock; Made in Costa Rica; Product Inquiries should be directed to Hospira, Inc., Lake Forest, IL 60045 USA; *** 3) List Number 046419701 labeled in part...
Source: Medical Device Recalls - March 7, 2014 Category: Medical Equipment Source Type: alerts

Boston Scientific Corporation - Boston Scientific Twister PLUS - Class 2 Recall
TWISTER¿ PLUS 26mm Rotatable Retrieval Device (Box of 5 configuration) Universal Product Number (UPN):M00561421. Distributed by: Boston Scientific, Natick, MA. Manufactured by: Horizons International Corp., Costa Rica. Intended to be used in flexible endoscopes as a retrieval device for foreign body objects, such as polyps and food boluses. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2014 Category: Medical Equipment Source Type: alerts

Hospira Inc. - Plum Blood Set - Class 1 Recall
List No. 14211-28; PLUM BLOOD SET; Prepierced Port, 200 Micron Filter, 110 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - Plum YType Blood Set - Class 1 Recall
List No. 14212-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - Blood Set - Class 1 Recall
List No. 14203-28; BLOOD SET; 200 Micron Filter, 80 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - Secondary Blood Set - Class 1 Recall
List No. 14200-28; SECONDARY BLOOD SET; 200 Micron Filter, 36 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - YType Blood Set - Class 1 Recall
List No. 14217-28; Y-TYPE BLOOD SET; 200 Micron Filter, Prepierced Y-Site, Non-Vented, 80 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - Plum Blood Set - Class 1 Recall
List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, Non-Vented, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - YType Blood Set - Class 1 Recall
List No. 14206-28; Y-TYPE BLOOD SET; 200 Micron Filter, Cylinder Pump, Convertible Pin and Non-Vented Pin, 80 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - YType Blood Set - Class 1 Recall
List No. 14219-28; Y-TYPE BLOOD SET; 200 Micron Filter, Cylinder Pump, CLAVE Y-Site, Non-Vented, 80 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - Blood Set - Class 1 Recall
List No. 14207-28; BLOOD SET; 200 Micron Filter, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2013 Category: Medical Equipment Source Type: alerts

Hospira Inc. - LifeShield Symbiq Set - Class 2 Recall
LifeShield; Sterile; Rx only; List No. 19666-28; SYMBIQ PUMP SET, CONVERTIBLE PIN, PIGGYBACK, 2 CLAVES PORTS AND OPTION LOK, NON-DEHP; NOMINAL LENGTH: 97 IN (249 CM); PRIMING VOLUME: 14 ML; For the administration of I.V. fluids; Made in Costa Rica; Hospira, Inc., Lake Forest, IL 60045 USA The Hospira Symbiq Infusion System is a general infusion system which provides IV infusion across the general spectrum of clinical care. The Symbiq pumps are standard sized pumps which are typically facility-based infusion pumps which may be used to deliver continuous and/or intermittent infusions to a variety of patient populations. (So...
Source: Medical Device Recalls - July 18, 2013 Category: Medical Equipment Source Type: alerts