Summary
The FDA issued a Class I for Impella RP Flex with SmartAssist; Product Number: 1000323; by Abiomed, Inc.. Reason: Optical Sensors have been damaged due to physical interaction between the inlet and another device resulting in a Placement Signal Not Reliable (PSNR).
Details
Source
Device Recall
External ID
Z-0830-2025
Action Date
2025-01-22
Status
Ongoing
Category
device
Product Description
Impella RP Flex with SmartAssist; Product Number: 1000323;
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437800, 438778, 437792, 437801, 438769, 437793, 436512, 436508, 436510, 436515, 436877, 436879, 436880, 436873, 436874, 436506, 436507, 436509, 436514, 436876, 436881, 437523, 436511, 436501, 436504, 436505, 436500, 436503, 436498, 437788, 437791, 434516A, 437540, 437783, 437784, 437786, 437561, 437558, 434512, 437535, 434510, 434511, 436093, 433954, 434517, 433949, 436101, 433952, 433953, 436094, 437541, 434508, 434831, 436096, 436098, 436100, 437537, 437536, 437539, 437538, 436092, 436097, 434513, 437529, 433955, 434514, 434515, 434805, 436148, 433751, 433748, 434808, 436146, 434799, 436151, 436149, 436150, 436143, 434837, 436145, 434832, 434838, 434834, 434836, 436142, 434833, 433923, 433926, 434830, 433925, 434806, 433927, 434801, 434800, 434802, 434803, 433753, 432652, 433749, 433752, 433754, 434543, 434545, 434546, 433757, 434538, 434541, 434542, 433755, 433756, 434540, 432645, 432646, 432648, 432643, 432644, 429654, 429652, 432650, 432651, 429653A, 432400, 432401, 432402, 432397, 432398, 429646, 429648, 429650, 429649, 429651, 430363, 430366, 430362, 430367, 430365, 432394, 432396, 430360, 432393, 432395, 431848, 431847, 431846, 431845, 431536, 431844, 431851, 431868, 431870, 431537, 431849, 431850, 431869, 431535, 431843, 431531, 431529, 431530, 431532, 431533, 431534, 431099, 431101, 431098, 431103, 428725, 431106, 431105, 431104, 428730, 428731, 428733, 428726, 428729, 428734, 425591, 425592, 425593, 425595, 425596, 425599, 430927, 430929, 430931, 425600, 429616, 429617, 429619, 429620, 430922, 430923, 430924, 429621, 430926, 429623, 424002, 424006, 424000, 424004, 424007, 422974, 422975, 422978, 422979, 422972, 423999, 423998, 424001, 422981, 422980, 418933, 418935, 418937, 418939, 418934, 418938, 418941, 418940, 419490, 419491, 419496, 421953, 419489, 419495, 421955, 419494, 420695, 420696, 420697, 421960, 420698, 420699, 421958, 421952, 421957, 421956, 409537, 409541, 409543, 409544, 409546, 416645, 416646, 416653, 416644, 416650, 409542, 416647, 416649, 416651, 411373, 411374, 411376, 411377, 411372, 411378, 411379, 411380, 410413, 410411, 410412, 410408, 410409, 410405, 410410, 410406, 410407, 407255A, 407988A, 407991A, 407989A, 407994A, 407253A, 407992A;
Quantity Affected: 2,364 units
Reason for Recall
Optical Sensors have been damaged due to physical interaction between the inlet and another device resulting in a Placement Signal Not Reliable (PSNR) alarm and loss of Central Venous (CV) Placement Signal, Pulmonary Artery (PA) Placement Signal & Pulmonary Artery Pulse Index (PAPi) metrics. Abiomed is reinforcing that there is a risk of potential interaction between the tip of guidewires, indwelling central venous lines or devices and inlet of the Impella pumps listed above during the insertion, manipulation, and removal of those devices. The interaction may result in optical sensor damage, temporary pump stop, or permanent pump stop.
Distribution
Domestic: Nationwide Distribution International: Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-12
Company
Danvers, MA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 249 device recalls issued in the same week, part of 413 device-related FDA actions this month.
Abiomed, Inc. has 66 FDA actions in our database, including 61 recalls and 5 clearances.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Abiomed, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Abiomed, Inc. have FDA actions?
Abiomed, Inc. has 66 FDA actions in our database, including 61 recalls and 5 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0830-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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