Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic…
Medical device recall Z-1934-2026. Published in FDA’s Enforcement Report on May 13, 2026.
- 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 May 13, 2026. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 11,253 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?
Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a variety of French sizes, endhole sizes, lengths, materials and designs (e.g., polyethylene or nylon, non-braided or braided with 1:1 torque). The choice of catheter material for different angiographic procedures should be based on the physician s experience.
11,253, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
UDI-DI 00827002119161 Lots 16905390 16905390X 16888263 NS16888264 16905391 16905391X 16909577 16918137 16924645 16924646 16928311 16928311X 16928312 16928313 16947353 16899656 16899655 16894976 16879299 16890985 16903201 16885859 16890986…
Every code shown here, 1,996 characters
UDI-DI 00827002119161 Lots 16905390 16905390X 16888263 NS16888264 16905391 16905391X 16909577 16918137 16924645 16924646 16928311 16928311X 16928312 16928313 16947353 16899656 16899655 16894976 16879299 16890985 16903201 16885859 16890986 16890982 16888268 16904428 16899658 16903202 16903203 16903204 16905389 16888267 16890983 16888269 16890981 16879296 16864346 16879301 16888261 16864344 16864351 16846774 16869144 16879300 16864350 16869143 16869143X NS16861721 16879297 16861735 16864347 16864347X 16882666 16899657 16890984 16899659 16888266 16861729 16857145 16858460 16857141 16861730 16861724 16858463 16852206 16855698 16858458 16858461 16858462 16858462X 16861726 16861727 16861728 16852209 16855686 16855696 16857146 16859718 16861720 16861723 16861725 16857137 16857142 16857139 16857140 16877835 16864345 16882665 16864353 16864348 16865462 16865462X 16879302 16843256 16833320 16843258 16845235 16845236 16839886 16845242 16845244 16845223 16845223X 16845226 16846777 16845230 16845227 16833315 16845218 16845246 16845233 16846778 16845229 16845240 16846779 16845241 16855694 16851384 16855695 16852208 16855693 16855697 16852207 16851381 16861733 16852711 16855688 16849691 NS16845220 NS16845220X 16846771 16846776 16845231 16851379 16851378 16851374 16846775 16851376 16855690 16849688 16846770 16846773 16861731 16861731X 16861732 16864352 16864354 NS16861722 16857144 16855691 16855692 16846772 16851380 16861734 16861734X 16864349 16851382 16857143 16857143X 16833228 16833298 16833292 16833321 16845239 16836838 16839887 16823055 16807168 16816808 16823045 16833290 16833299 16836839 16836839X 16833316 16833314 16833310 16823062 16823062X 16825484 16833229 16833230 16833231 16833232 16833289 16833307 16833308 16833309 16833311 16833312 16833313 16833296 16845237 16802095 16833301 16833302 16843254 16843255 16843257 16845234 16833297 16833293 16833304 16833300 16802091 16802091X 16833291 16833303 16800397 16800399 16802092 16823046 16823047 16823048 16823049 16823050…
FDA’s list runs to 4,570 characters. The first part is shown; the rest is on FDA’s record.
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 distribution nationwide. OUS distribution to Brunei, Brazil, Canda, China, Colombia, Costa Rica, Hong Kong, Israel, India, Japan, South Korea, Macau, New Zealand, Singapore, El Salvador, Taiwan, Uruguay
These words name no state.
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?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 2, 2026.
- FDA classified it on May 1, 2026.
- FDA’s Enforcement Report published it on May 13, 2026.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Cook Incorporated, 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.”
- FDA’s list of codes runs to 4,570 characters; the first part is shown here, and the rest is on FDA’s record.
- 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.