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Devices
Device Recall Mar Cor Purification Reverse Osmosis System
Model / Serial
serial numbers: 1289064, 1289069, 1289159, 1289259, 1289387, 1289650, 1289747, 1289826, 1289949, 1290088, 1290151, 1290333, 1290367, 1290480, 1290489, 1290845, 1290988, 1291042, 1291120, 1291233, 1291373, 1291378, 1291634, 1291777, 1291828, 1291933, 1292031, 1292114, 1292185, 1292185, 1292192, 1292391, 1292546, 1292597, 1292670, 1292674, 1292899, 1292960, 1293010, 1293039, 1293185, 1293190, 1293311, 1293379, 1293414, 1293687, 1293724, 1293771, 1293777, 1293953, 1293957, 1294093, 1294103, 1294171, 1294307, 1294362, 1294433, 1294516, 1294589, 1294727, 1294864, 1294999, 1295113, 1295137, 1295160, 1295186, 1295274, 1295391, 1295514, 1295622, 1295813, 1295871, 1296237, 1296241, 1296246, 1296484, 1296491, 1296582, 1296621, 1296650, 1296695, 1296806, 1297041, 1297046, 1297118, 1297231, 1297234, 1297372, 1297375, 1297394, 1297453, 1297484, 1297610, 1297655, 1297939, 1297943, 1298037, 1298210, 1298266, 1298270, 1298377, 1298407, 1298450, 1298457, 1298575, 1298619, 1298624, 1298704, 1298734, 1298797, 1298820, 1298879, 1298913, 1298952, 1298953, 1299037, 1299120, 1299144, 1299170, 1299241, 1299262, 1299285, 1299331, 1299393, 1299473, 1299512, 1299599, 1299655, 1299656, 1299732.
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
nationwide. No distribution outside the US.
Product Description
Mar Cor Purification CWP Reverse Osmosis System. Models 101, 102, 104, and 106.
Manufacturer
Mar Cor Purification
1 Event
Recall of Device Recall Mar Cor Purification Reverse Osmosis System
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Manufacturer
Mar Cor Purification
Manufacturer Address
Mar Cor Purification, 14550 28th Ave N, Minneapolis MN 55447-4817
Manufacturer Parent Company (2017)
Cantel Medical Corp.
Source
USFDA
Language
English
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