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U.S. Department of Health and Human Services

Class 2 Device Recall Impella CP Smart Assist

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 Class 2 Device Recall Impella CP Smart Assistsee related information
Date Initiated by FirmAugust 05, 2024
Date PostedSeptember 04, 2024
Recall Status1 Open3, Classified
Recall NumberZ-2969-2024
Recall Event ID 95129
Product Classification Temporary non-roller type left heart support blood pump - Product Code OZD
ProductImpella CP Smart Assist Set; Product Code: 1000402;
Code Information Product Code: 1000402; UDI-DI: 00813502012873; Serial Numbers: 385946 385942 385944 385945 385950 385941 385949 385947 385948 385943 392855 392853 392854 392852 392851 392848 392849 392879 392878 427388 427387 427386 430896 430875 430874 430873 430872 430871 430870 430869 430868 430867 431652 430895 430894 486297 486298 486299 486300; Batch Numbers: 2023251705 2023251861 2023251862 2023251869 2023251872 2023251874 2023251876 2023251879 2023251881 2023251902 2023283187 2023283192 2023283194 2023283196 2023283200 2023283208 2023283216 2024305462 2024305463 2024305465 2024305466 2024305467 2024308137 2024308138 2024308139 2024308141 2024308143 2024308144 2024308146 2024308148 2024308149 2024308150 2024308159 2024308160 2024308162 2025501277 2025501292 2025501297 2025501301;
Recalling Firm/
Manufacturer		 Abiomed, Inc.
24 Cherry Hill Dr
Danvers MA 01923-2575
For Additional Information ContactMorgaine Johnson
612-437-5734
Manufacturer Reason
for Recall		A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.) content related to this potential interaction, so Abiomed will update the IFU to include information on this potential device interaction.
FDA Determined
Cause 2		Under Investigation by firm
ActionOn August 5, 2024 URGENT MEDICAL DEVICE CORRECTION (NOTIFICATION) letters were sent to consignees. ACTIONS TO BE TAKEN BY CUSTOMER/USER: " Product is NOT being removed from the field and does not need to be returned. " Review, complete all fields, sign, and return the attached business response form (BRF) (refer to Attachment 2) to Abiomed2860@SEDGWICK.COM. " Forward this notice to anyone in your facility that needs to be informed (i.e., those who manage, transport, store, stock, or use the subject products). " If any of the subject products have been forwarded to another facility, contact that facility and provide them with this notice. " Post a copy of this notice in a visible area for awareness of this field safety notice. " As with any medical device, adverse reactions or quality problems experienced with the use of this product should be reported to the FDA s MedWatch Adverse Event Reporting Program using the link below: https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program/reporting-serious-problems-fda At Abiomed, our priority is to our customers and their patients, and that includes the safe and effective use of our products. If you have questions or concerns regarding this notice, please contact your local clinical field staff. Thank you for your cooperation.
Quantity in Commerce39 units
DistributionWorldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Brazil, Brunei Darussalam, Canada, Croatia, Czeck Republic, Denmark, Finland, France, Germany, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Luxembourg, Malaysia, Mexico, Netherlands, Norway, Panama, Poland, Saudi Arabia, Serbia, Singapore, Slovenia, Spain, Sweden, Switzerland, Taiwan, U.A.E., United Kingdom.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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