Devices

Device Recall AMPLATZER Delivery Systems

Model / Serial
M01J19-12, M02B14-10, M02C12-27, M02D16-19, M02D16-23 M02F24-07, M02G23-04, M02H19-05, M02K07-48, M02K12-10 M02L11-13, M03A09-13, M03A20-11, M03A20-18, M03A22-12 M03B10-56, M03B20-11, M03C24-13, M03D08-08, M03D16-18 M03E27-08, M03F13-07, M03F18-10, M03H12-43, M03J04-12 M03J19-08, M03J25-27, M03K09-23, M03K28-36, M03L11-46 M03M03-12, M03M29-07, M04A19-28, M04A28-16, M04B03-13 M04B09-19, M04B17-33, M04B24-08, M04C23-11, M04D06-13 M04D26-06, M04D26-10, M04F08-22, M04F28-47, M04H24-22 M04J07-09, M04J10-22, M04J17-08, M04K15-10, M04L02-02
Distribution
Product has been distributed throughout the US and Internationally, including Canada, Europe and Australia.
Product Description
AMPLATZER Delivery System 45-degree curve, order no. 9-DEL-8F-45/80. Product is labeled as Sterile EO. || Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchange Systems are placed onto polyboard backing cards. The backing card is then placed into a smaller of 2 Tyvek pouches. The pouch is then placed inside a larger Tyvek pouch. The kit is assembled at AGA and then sterilized by Steris, Minneapolis, MN.
Manufacturer
AGA Medical Corporation
1 Event
- Recall of Device Recall AMPLATZER Delivery Systems

Manufacturer

AGA Medical Corporation

Manufacturer Address
AGA Medical Corporation, 682 Mendelssohn Ave N, Golden Valley MN 55427-4306
Source
USFDA

12 devices with a similar name

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Device Recall AMPLATZER Delivery Systems

Model / Serial
00E01-13, M02K07-44, M03C24-17, M03E27-07, M03F18-09, M03L11-45, M04B09-16, M04E27-19
Distribution
Product has been distributed throughout the US and Internationally, including Canada, Europe and Australia.
Product Description
Amplatzer Delivery Systems (45-degree curve). order no. 9-DEL-6F-45/60. Product is labeled as Sterile EO. || Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchang Systems are placed onto polyboard backing cards. The backing card is then placed into a smaller of 2 Tyvek pouches. The pouch is then placed inside a larger Tyvek pouch. The kit is assembled at AGA and then sterilized by Steris, Minneapolis, MN.
Manufacturer
AGA Medical Corporation

Device Recall AMPLATZER Delivery Systems

Model / Serial
M01J08-12, M02D26-01, M02L11-20, M03A09-12, M03B20-12, M03D16-24, M03F18-08, M03L12-09, M04C23-09, M04G01-24
Distribution
Product has been distributed throughout the US and Internationally, including Canada, Europe and Australia.
Product Description
AMPLATZER Delivery System 45-degree curve, order no. 9-DEL-7F-45/60. Product is labeled as Sterile EO. || Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchange Systems are placed onto polyboard backing cards. The backing card is then placed into a smaller of 2 Tyvek pouches. The pouch is then placed inside a larger Tyvek pouch. The kit is assembled at AGA and then sterilized by Steris, Minneapolis, MN.
Manufacturer
AGA Medical Corporation

Device Recall AMPLATZER Delivery Systems

Model / Serial
M01K01-6, M02C12-24, M02C25-15, M02F05-23, M02F24-05, M02L02-21, M03A09-10, M03A09-15, M03A20-10, M03B20-17 M03C24-14, M03F02-17, M03G23-08, M03H12-42, M03J19-07 M03K14-06, M03K28-35, M03L11-48, M04B03-09, M04B03-14 M04C08-12, M04D06-12, M04E11-28, M04E24-20, M04F08-23 M04H03-23, M04J17-07, M04K07-02
Distribution
Product has been distributed throughout the US and Internationally, including Canada, Europe and Australia.
Product Description
AMPLATZER Delivery System 45-degree curve, order no. 9-DEL-7F-45/80. Product is labeled as Sterile EO. || Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchange Systems are placed onto polyboard backing cards. The backing card is then placed into a smaller of 2 Tyvek pouches. The pouch is then placed inside a larger Tyvek pouch. The kit is assembled at AGA and then sterilized by Steris, Minneapolis, MN.
Manufacturer
AGA Medical Corporation

Device Recall AMPLATZER Delivery Systems

Model / Serial
M02D26-02, M02I23-02, M02J10-09, M02K07-47, M03C04-06 M03D16-16, M03F18-07, M03K14-07, M03L18-50, M03M03-11 M04C23-10, M04E24-18, M04G01-20
Distribution
Product has been distributed throughout the US and Internationally, including Canada, Europe and Australia.
Product Description
AMPLATZER Delivery System 45-degree curve, order no. 9-DEL-8F-45/60. Product is labeled as Sterile EO. || Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchange Systems are placed onto polyboard backing cards. The backing card is then placed into a smaller of 2 Tyvek pouches. The pouch is then placed inside a larger Tyvek pouch. The kit is assembled at AGA and then sterilized by Steris, Minneapolis, MN.
Manufacturer
AGA Medical Corporation

Device Recall AMPLATZER Delivery Systems

Model / Serial
M01L17-02, M02A28-21, M02A28-24, M02K07-46, M03G10-30, M03L18-52, M04B09-18, M04C23-13, M04E27-20, M04F08-24, M04H03-20, M04K26-18
Distribution
Product has been distributed throughout the US and Internationally, including Canada, Europe and Australia.
Product Description
AMPLATZER Delivery System 180-degree curve, order no. 9-DEL-8F-180/80. Product is labeled as Sterile EO. || Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchange Systems are placed onto polyboard backing cards. The backing card is then placed into a smaller of 2 Tyvek pouches. The pouch is then placed inside a larger Tyvek pouch. The kit is assembled at AGA and then sterilized by Steris, Minneapolis, MN.
Manufacturer
AGA Medical Corporation

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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