Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106
Medical device recall Z-1563-2014. Published in FDA’s Enforcement Report on May 14, 2014.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on May 14, 2014. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 38 states named
- 197 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Mar Cor Purification manufactured Central Water Plant (CWP) reverse osmosis system, models 102, 104 and 106. This correction has been initiated due to a potential situation with a specific lot of the water inlet solenoid valve. The potential exists that the water inlet solenoid valve could cease to function. If this occurs, CWP will stop producing reverse osmosis water.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse osmosis system with the intended use of producing water for dialysis of multiple patients.
197, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
1301273 1302515 1303486 1304517 1305636 1306626 1307463 1308631 1309375 1301350 1302516 1303487 1304571 1305711 1306666 1307536 1308665 1309437 1301453 1302600 1303559 1304660 1305782 1306666 1307758 1308666 1309532 1301456 1302634 1303560…
Every code shown here, 1,575 characters
1301273 1302515 1303486 1304517 1305636 1306626 1307463 1308631 1309375 1301350 1302516 1303487 1304571 1305711 1306666 1307536 1308665 1309437 1301453 1302600 1303559 1304660 1305782 1306666 1307758 1308666 1309532 1301456 1302634 1303560 1304662 1305840 1306718 1307759 1308722 1309566 1301514 1302655 1303680 1304750 1305907 1306722 1307841 1308799 1309589 1301580 1302675 1303722 1304794 1305953 1306810 1307842 1308821 1309592 1301682 1302703 1303728 1304851 1305954 1306834 1307857 1308830 1309613 1301705 1302714 1303776 1304962 1306107 1306844 1307897 1308833 1309647 1301751 1302791 1303839 1305045 1306108 1306897 1307904 1308981 1309662 1301898 1302809 1303840 1305108 1306110 1306913 1308035 1309027 1309717 1301966 1302852 1303876 1305142 1306225 1307022 1308052 1309029 1309743 1301972 1302933 1303943 1305176 1306228 1307041 1308059 1309120 1309765 1302063 1302934 1303977 1305193 1306299 1307041 1308201 1309123 1309807 1302074 1302993 1304027 1305234 1306307 1307042 1308202 1309139 1309860 1302115 1302994 1304112 1305303 1306308 1307095 1308217 1309206 1309890 1302195 1303055 1304158 1305341 1306377 1307219 1308279 1309227 1309904 1302266 1303144 1304176 1305342 1306411 1307230 1308294 1309241 1309923 1302269 1303178 1304235 1305379 1306465 1307276 1308335 1309280 1309926 1302319 1303231 1304286 1305472 1306467 1307317 1308384 1309283 1309983 1302337 1303232 1304428 1305523 1306544 1307391 1308443 1309327 1310113 1302461 1303322 1304440 1305632 1306599 1307413 1308520 1309364 1310147 1302485 1303391 1304454 1305633 1306610 1307418 1308533 1309374
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US Nationwide Distribution - AL, AZ, AR, CA, CO, FL, GA, ID, IN, IA, KS, KY, LA, MA, MI, MN, MS, MO, MT, NH, NJ, NM, NY,NC, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WV, WI.
The states and territories these words name
38 states and territories.
Every one of them
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Florida
- Georgia
- Iowa
- Idaho
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- New Hampshire
- New Jersey
- New Mexico
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Puerto Rico
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Washington
- Wisconsin
- West Virginia
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Apr 24, 2014.
- FDA classified it on May 6, 2014.
- FDA’s Enforcement Report published it on May 14, 2014.
- FDA terminated it on Nov 20, 2015.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Mar Cor Purification, of Minneapolis, MN.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.