Medtronic Vascular, Inc. recalls Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF ENBF2313C120EE;…
Stent Graft Systems built with specific batches of taper tip assemblies have the potential for the taper tip to detach from the delivery system. Detachment of the taper tip during the implant procedure may lead to a…
Read the official notice →- Date
- 2022-03-02
- Country
- United States
- Brand
- Medtronic Vascular
- Product
- Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF ENBF2313C120EE; ENBF2313C120EE;…
- Classification
- Class II
- Units
- Worldwide distribution - U.S. Nationwide distribution in the states of AK, AL,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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Medtronic Vascular, Inc. recalls Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE STENT GRAFT…
Due to, during stent graft deployment, the spindle may detach from the distal end of the spindle hypotube.
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During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube
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Other drugs & medical recalls in the United States
- 2022-03-02
- US
Natus Neurology DBA Excel Tech., Ltd. (XLTEK) recalls IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
Tile kits that allow one to install and situate a video camera within a patient environment are not fitting properly in some domestic institution ceiling tile grids that have a thinner style grid frame. The ceiling…
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BALT USA, LLC recalls The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to a proximal…
Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf carton label or pouch label due to inadequate manufacturing line clearance. As a result of this labeling mix-up, there is the possibility of…
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Nobel Biocare Usa Llc recalls NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
Due to 16 complaints related to drivers not engaging in implants. According to the firm's investigations, the incorrect offset gauge was potentially used during production of the implants. As a result, this could…
FDA · DeviceNobel Biocare Usa LlcWorldwide distribution - U.S. Nationwide distribution in the states of AL, AR,…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Michels Transport Medium, 20ML Prefilled Cont
Product stored incorrectly in temperature controlled setting instead of refrigeration.
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AMS Packaging Inc recalls Premium Nature Instant Hand Sanitizer, (ethyl alcohol 70%), plastic bottle packaged as (a) 8 OZ, UPC 8 19192 02866 8; (b) 16 OZ, UPC 8…
Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
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Positive Health recalls RISE UP RED EDITION Capsules, 650 mg, 10-count blisters packaged in a carton, ASIN B08JCWG84D, barcode X002NI8PE1.
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FDA · DrugPositive HealthProduct was distributed nationwide via the internet through Amazon Marketplace.Official notice →