BioFlo PICC and Xcela PICC Convenience Kits - Product Usage: are indicated for short or long-term peripheral…
Medical device recall Z-2397-2020. Published in FDA’s Enforcement Report on Jun 24, 2020.
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 Jun 24, 2020. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 119723 eaches total 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?
Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
BioFlo PICC and Xcela PICC Convenience Kits - Product Usage: are indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications and nutrients; the sampling of blood; and for power injection of contrast media. Item Numbers H96560M01162101 H96560M0116291 H96560M0133531 H96560M0134211 H96560M0198811 H96560M0224741 H96560M0224751 H96560M0335621 H96560M0367041 H96560M0367051 H96560M0367061 H96560M05019111 H96560M0501981 H96560M1201961 H96560M1201971 H96560M12202101 H96560M12202111 H96560M12202121 H96560M1303151 H96560M1303171 H96560M1303191 H96560M13184101 H96560M13184111 H96560M1318491 H96560M1401411 H96560M1401421 H96560M1401431 H96560M1401441 H96560M1406061 H96560M1406071 H96560M1633931 H96560M1803441 H96560M1803451 H96560M18157111 H96560M18157121 H96560M1841151 H96560M1841161 H96560M1841171 H96560M1907131 H96560M1907141 H96560M2204441 H96560M2208511 H96560M2208521 H96560M2322421 H96560M2500961 H96560M2500971 H96560M610115911 H96560M610901011 H96560M611025121 H96560M611025131 H96560M611052821 H96560M611056021 H96560M611056031 H96560M611095821 H96560M611095831 H965PKM030667S1 H965PKM120451S1 H965PKM1220226S1 H965PKM1300011S1 H965PKM1303119S1 H965PKM131935S1 H965PKM150124S1 H965PKM150125S1 H965PKM150127S1 H965PKM220851S1 H965PKM220854S1 H965PKM3092662S1 H965PKM61040701S1 H965PKM61066141S1 H965PKM61095321S1 H965PKM61095324S1 Cat. No. 60M0116210 60M011629 60M013353 60M013421 60M019881 60M022474 60M022475 60M033562 60M036704 60M036705 60M036706 60M0501911 60M050198 60M120196 60M120197 60M1220210 60M1220211 60M1220212 60M130315 60M130317 60M130319 60M1318410 60M1318411 60M131849 60M140141 60M140142 60M140143 60M140144 60M140606 60M140607 60M163393 60M180344 60M180345 60M1815711 60M1815712 60M184115 60M184116 60M184117 60M190713 60M190714 60M220444 60M220851 60M220852 60M232242 60M250096 60M250097 60M61011591 60M61090101 60M61102512 60M61102513 60M61105282 60M61105602 60M61105603 60M61109582 60M61109583 PKM030667S PKM120451S PKM1220226S PKM1300011S PKM1303119S PKM131935S PKM150124S PKM150125S PKM150127S PKM220851S PKM220854S PKM3092662S PKM61040701S PKM61066141S PKM61095321S PKM61095324S
119723 eaches total, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Lots 5502064 5499646 5537999* 5470193 5482411 5491837 5498227 5519222 5523176 5534734 5544000 5574435 5583228 5468490 5485176 5525973 5552143 5569544 5476092 5482007 5474457 5498239 5513077 5532408 5555127 5574431* 5465977 5474459 5491848…
Every code shown here, 1,996 characters
Lots 5502064 5499646 5537999* 5470193 5482411 5491837 5498227 5519222 5523176 5534734 5544000 5574435 5583228 5468490 5485176 5525973 5552143 5569544 5476092 5482007 5474457 5498239 5513077 5532408 5555127 5574431* 5465977 5474459 5491848 5513071 5534738 5559194 5576291* 5470199 5480504 5491841 5513063 5528679 5566358 5576283 5498237 5546409 5468510 5487221 5528681 5537991 5566360 5574447 5586266 5587813 5465983 5474461 5487219 5491856 5502075 5519230 5546399 5555117 5574427 5587267 5530190 5460247 5468506 5478056 5498235 5519224 5530200 5546405 5557541 5569536 5574437 5578568 5488823 5502081 5465979 5468518 5485174 5488829 5502073 5519228 5530187 5548446 5559211 5566366 5574429 5578562 5583236 5474465 5546403 5468494 5474455 5485180 5502067 5525966 5537993 5555121 5559200 5566368 5578551 5488821 5496910 5569546 5585539* 5472110 5480506 5487225 5498231 5505007 5523171 5532396 5555131 5559204 5567557 5576293 5583232 5588904 5491844 5548431 5465975 5478054 5502060* 5530198* 5463223 5468502 5502058* 5471177 5484653 5490779 5499462 5497832 5496904 5502069 5532406 5559198 5588906* 5468498 5491846 5513056 5525993 5530194 5538001 5543992 5548448 5555133 5564678 5567555* 5580574* 5477981 5482407 5530196 5536952 5548440 5557551 5571892 5574441 5564684 5589187* 5541640 5574117 5477985 5482409 5492430 5530268 5536954 5574443 5557547 5569538 5583230* 5585537* 5460261 5468500 5478052 5482403 5488817 5498223 5502071 5525986 5532400 5566362 5571890 5576273 5552141 5548438 5569540 5583214 5496380 5500241 5564686 5465971 5478048 5485170 5488813 5502079 5576281 5583226 5496902 5465981 5472108 5496914 5500251 5502083 5534736 5544004 5576289 5552135 5566347 5583234* 5491406 5494896 5497840 5500245 5481600 5487425 5491408 5496883 5498249 5500239 5497842 5488166 5491404 5497843 5552091 5494898 5500247 5463219 5480498 5487217 5513054 5525971 5528674 5557549 5576285 5580568 5546407 5564680 5583217* 5480497 5487211 5513061 5528672 5559202 5566341 5576295 5504997 5546413 5585293 5538003…
FDA’s list runs to 3,310 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 Nationwide distribution.
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.
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 May 4, 2020.
- FDA classified it on Jun 17, 2020.
- FDA’s Enforcement Report published it on Jun 24, 2020.
- FDA terminated it on Aug 23, 2023.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Angiodynamics, Inc., of Queensbury, NY.
- 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 3,310 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
-
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.