Slip-Cath Beacon Tip Catheter. Angiographic catheter. recall
Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help…
Why was Slip-Cath Beacon Tip Catheter. Angiographic catheter. recalled?
Reports of catheter tip splits and or separation. Loss of device function, medical intervention to retrieve separated segment, or complications resulting from separated tip occluding blood flow to end organs may result.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All lots of the following Product numbers: SCBR4.0-35-150-P-NS-0, SCBR4.0-35-65-P-NS-RC2, SCBR4.0-38-100-P-NS-0, SCBR4.0-38-100-P-NS-C2, SCBR4.0-38-100-P-NS-DAV, SCBR4.0-38-100-P-NS-H1, SCBR4.0-38-100-P-NS-HN4, SCBR4.0-38-100-P-NS-JB1, SCBR4.0-38-100-P-NS-JB2, SCBR4.0-38-100-P-NS-KMP, SCBR4.0-38-100-P-NS-MAN, SCBR4.0-38-100-P-NS-MPA, SCBR4.0-38-100-P-NS-MPB, SCBR4.0-38-100-P-NS-SIM1, SCBR4.0-38-100-P-NS-SIM2, SCBR4.0-38-100-P-NS-SIM3, SCBR4.0-38-100-P-NS-VERT, SCBR4.0-38-125-P-NS-0, SCBR4.0-38-125-P-NS-DAV, SCBR4.0-38-125-P-NS-JB1, SCBR4.0-38-125-P-NS-SIM1, SCBR4.0-38-125-P-NS-SIM2, SCBR4.0-38-125-P-NS-TEGT, SCBR4.0-38-125-P-NS-VERT, SCBR4.0-38-125-P-NS-VTK, SCBR4.0-38-40-P-NS-KMP, SCBR4.0-38-65-P-NS-0, SCBR4.0-38-65-P-NS-C2, SCBR4.0-38-65-P-NS-KMP, SCBR4.0-38-65-P-NS-MPA, SCBR4.0-38-65-P-NS-RIM, SCBR4.0-38-65-P-NS-TC, SCBR4.0-38-65-P-NS-TC-BNK, SCBR4.0-38-65-P-NS-VERT, SCBR4.0-38-80-P-NS-RH, SCBR4.0-38-80-P-NS-VS, SCBR4.0-38-80-P-NS-VS1, SCBR4.0-38-80-P-NS-VS2, SCBR4.0-38-80-P-NS-VS3, SCBR4.1-35-65-P-NS-C2, SCBR4.1-35-75-P-NS-CHG2.5, SCBR5.0-35-90-P-NS-RUC
- Product
- Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help…
- Recalling firm
- Cook Inc.
- Quantity
- 248167
- Distribution
- Worldwide Distribution - US (nationwide including Puerto Rico and US Virgin Islands), Algeria, Antigua, Armenia, Austria, Australia, Bahamas, Belgium, Bangladesh, Bulgaria, Bahrain, Brazil, Brunei Darussalam, Canada, Canary Islands, Chile, China, Colombia, Costa Rica, Cyprus, Czech Republic, Denmark, Dominican Republic, Egypt, El Salvador, Finland, France, French Polynesia, Georgia, Germany, Ghana, Great Britain, Greece Guadeloupe, Hong Kong, Hungary, Iceland, India, Indonesia, Iraq, Ireland, Israel, Italy, Japan, Jersey, Jordan, Kuwait, Kazakhstan, Republic of Korea, Kuwait, Lebanon, Lithuania, Luxemburg, Latvia, Libya, Macau, Malaysia, Malta, Martinique, Mexico, Mongolia, Morocco, Netherlands, Netherlands Antilles, New Caledonia, New Zealand, Nicaragua, Norway, Oman, Pakistan, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Sri Lanka, Sweden, Switzerland, Spain, Taiwan, Thailand, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, and Vietnam.
- Recall date
- August 12, 2015
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)