Radial Artery Pressure Monitoring Catheter Sets and Trays The subject sets and trays are comprised of a…
Medical device recall Z-0802-2016. Published in FDA’s Enforcement Report on Mar 2, 2016.
- FDA Class I
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 Mar 2, 2016. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 2 states named
- 12691 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 I, the most serious of FDA’s three classes.
“Dangerous or defective products that predictably could cause serious health problems or death. Examples include: food found to contain botulinum toxin, food with undeclared allergens, a label mix-up on a lifesaving drug, or a defective artificial heart valve.”
openFDA, in plain words, its enforcement report fields.
“Class I is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
FDA’s rule, 21 CFR 7.3(m)(1), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
A manufacturing process may lead to catheter tip fracture and or separation. Potential adverse events may include loss of device function, medical intervention to retrieve a separated segment, or complications resulting from a separated tip occluding blood flow to end organs. These catheters are used in venous or arterial pressure monitoring, blood sampling, and administration of drugs and fluids.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Radial Artery Pressure Monitoring Catheter Sets and Trays The subject sets and trays are comprised of a single-lumen uncoated or heparin-coated catheter. Product catalog numbers with heparin coating are designated by the suffix BH.
12691, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
RPN/Catalog number: C-PMS-250-RA C-PMS-251-RA C-PMS-300-RA C-PMS-300-RA-CHOP C-PMS-301J-RA C-PMS-301-RA C-PMS-400-RA C-PMSY-250-RA C-PMSY-300-RA C-PMSY-301-RA Lots: 6049998 6160195 6160212 NS5898558 NS6063328 NS6178204 NS6178206 5895605…
Every code shown here, 1,362 characters
RPN/Catalog number: C-PMS-250-RA C-PMS-251-RA C-PMS-300-RA C-PMS-300-RA-CHOP C-PMS-301J-RA C-PMS-301-RA C-PMS-400-RA C-PMSY-250-RA C-PMSY-300-RA C-PMSY-301-RA Lots: 6049998 6160195 6160212 NS5898558 NS6063328 NS6178204 NS6178206 5895605 6191185 5793196 5800313 5800443 5800569 5806981 5810905 5810917 5824484 5824546 5824547 5824548 5866984 5866985 5866986 5870319 5881447 5881519 5889496 5891905 5911486 5922847 5922848 5925742 5928632 5939446 5939447 5939448 5976502 6025016 6025094 6033768 6034981 6034983 6050000 6062738 6062742 6067675 6067676 6075206 6075207 6083936 6083954 6083985 6083986 6129056 6148790 6160236 6165591 6174974 6175289 6191362 6269150 NS6063331 NS6108226 NS6170739 NS6170767 5905252 6003109 NS6072553 5793197 5800571 5800572 5824485 5824551 5845063 5864072 5866988 5873125 5881151 5881152 5884641 5884642 5889464 5892063 5892064 5922850 5939431 5942091 5951549 5953768 5954322 5967404 5974281 5994817 5996926 6003161 6003162 6017048 6025095 6025145 6034984 6042699 6050002 6075210 6075211 6075212 6081723 6083988 6100756 6124809 6125111 6148791 6153122 6160239 6160240 6168131 6171368 6187477 6250532 6059759 NS6047396 NS6047397 NS6047398 NS6047399 NS6047440 NS6047442 6124812 5793192 5824526 5884647 5892068 5942090 5967410 6003167 6059765 6134128 6153124 6168137 6254068 5793193 5866995 5892069 5942092 6003168 6025099 6067664 6168138
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.
Worldwide Distribution - US Nationwide including DC and PR including the countries of Australia, Germany, China, Chile, Dominican Republic, Panama, Israel, Brazil, Canada
The states and territories these words name
- District of Columbia
- Puerto Rico
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.
The words say it went outside the United States too.
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 Jan 6, 2016.
- FDA classified it on Feb 24, 2016.
- FDA’s Enforcement Report published it on Mar 2, 2016.
- FDA terminated it on Aug 23, 2017.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Cook Inc., of Bloomington, IN.
- 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
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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.