Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel
Medical device recall Z-2303-2023. Published in FDA’s Enforcement Report on Aug 9, 2023.
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 Aug 9, 2023. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 100,549 kits 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?
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. VASCULAR PACK, Model Number: DYNJ22350K, DYNJ22350L, DYNJ22676J, DYNJ23445F, DYNJ31902L, DYNJ31902M, DYNJ39432I, DYNJ39432J, DYNJ39432K, DYNJ41625B, DYNJ46246A, DYNJ53438A, DYNJ53610C, DYNJ53995G, DYNJ56791A, DYNJ56791B, DYNJ57490A, DYNJ58608, DYNJ58681A, DYNJ58681B, DYNJ58710, DYNJ61325A, DYNJ61325B, DYNJ61528, DYNJ62399A, DYNJ65160, DYNJ66356, DYNJ66356A, DYNJ66356B, DYNJ66356C, DYNJ66356D, DYNJ66577, DYNJ68492A, DYNJ68492B, DYNJ68492C, DYNJ68492D, DYNJ68863, DYNJ68863A, DYNJ68880, DYNJ80599, DYNJ81626, DYNJ82016, DYNJ82104, DYNJ82144, DYNJ82769, DYNJ82769A, DYNJ83146; b. VASCULAR PACK CHRG, Model Number: DYNJ59778A, DYNJ59778B; c. VASCULAR PACK GWV, Model Number: DYNJ59245; DYNJ59245A; d. VASCULAR PACK MH-LF, Model Number: DYNJ39866B, DYNJ39866C; e. VASCULAR PACK SHD, Model Number: DYNJ68404; f. VASCULAR PACK-LF, Model Number: DYNJ0250564O, DYNJ0250564P, DYNJ0373040N, DYNJ0493141G, DYNJ0493141I, DYNJ0493141J, DYNJ0871182AC, DYNJ0901358I, DYNJ0901358J, DYNJ0901358K, DYNJ53475F, DYNJ53684A, PHS400047N, PHS400047O; g. VASCULAR STENT INOVA, Model Number: DYNJ906440A; h. VASCULAR TRAY, Model Number: DYNJ56858; i. VASCULAR/OR ANGIO, Model Number: DYNJ905079F; j. VASCULAR-LF, Model Number: DYNJ900714B, DYNJ900714C; k. VEIN ABLATION EXCISION ASC, Model Number: DYNJ52586B; l. VEIN ABLATION & EXCISION ASC, Model Number: DYNJ52586, DYNJ52586A, DYNJ52586B; m. VEIN ABLATION KIT, Model Number: DYNJ69272A; n. VEIN ABLATION PACK, Model Number: DYNJ62889; o. VEIN ABLATION TRAY W/CHLOR, Model Number: DYNJ64396; p. VEIN AND LASER PACK, Model Number: DYNJ49874; q. VEIN CENTER PACK, Model Number: DYNJ52123; r. VEIN CLINIC, Model Number: DYNJ68667; s. VEIN CLOSURE PACK, Model Number: DYNJ35586G, DYNJ39408F, DYNJ65189B; t. VEIN CLOSURE TRAY, Model Number: DYNJ44737B; u. VEIN KIT, Model Number: DYNJ57047; v. VEIN LIGATION, Model Number: DYNJ64190; w. VEIN OHH, Model Number: DYNJ65560A; x. VEIN PACK, Model Number: DYNJ21949J, DYNJ39005B, DYNJ39889, DYNJ48493, DYNJ48907F, DYNJ50785, DYNJ52098, DYNJ52993A, DYNJ53160, DYNJ53160A, DYNJ54153B, DYNJ55268, DYNJ55462A, DYNJ55514A, DYNJ55849A, DYNJ56624, DYNJ56724A, DYNJ56724B, DYNJ57512, DYNJ57835, DYNJ57917, DYNJ58063, DYNJ58609, DYNJ59151F, DYNJ59662B, DYNJ59662D, DYNJ59677A, DYNJ59681A, DYNJ61540C, DYNJ63823, DYNJ64282, DYNJ64471A, DYNJ65579, DYNJ66154, DYNJ66743A, DYNJ68749, DYNJ69091, DYNJ80199A, DYNJ80199B, DYNJ80868, DYNJ83147; y. VEIN PACK II, Model Number: DYNJ66427; z. VEIN PACK-LF, Model Number: DYNJ66271A, DYNJ66271C; aa. VEIN PROCEDURE, Model Number: DYNJ65342A; bb. VEIN PROCEDURE PACK, Model Number: DYNJ38264D, DYNJ62038A, DYNJ64909; cc. VEIN SPECIALISTS PACK, Model Number: DYNJ53616A; dd. VEIN TRAY, Model Number: DYNJ57003, DYNJ62829A; ee. VENOUS ABLATION, Model Number: DYNJ50227C; ff. VENOUS ACCESS ACCESSORY PACK, Model Number: DYNJ61010A; gg. VENOUS ACCESS PACK, Model Number: DYNJ44421D; hh. VIRC STROKE PACK, Model Number: DYNJ83461; ii. VNUS, Model Number: CDS984292I; jj. VNUS CLOSURE, Model Number: DYNJ66076; kk. VNUS VASCULAR PACK, Model Number: DYNJ66445; ll. WA VASCULAR PACK-LF, Model Number: DYNJ33612G
100,549 kits, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2023: a. Model Number: DYNJ22350K, UPC Number: 019348956435; Model Number: DYNJ22350L, UPC Number: 019348944525; Model…
Every code shown here, 1,999 characters
All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2023: a. Model Number: DYNJ22350K, UPC Number: 019348956435; Model Number: DYNJ22350L, UPC Number: 019348944525; Model Number: DYNJ22676J, UPC Number: 019348956435; Model Number: DYNJ23445F, UPC Number: 019532715035; Model Number: DYNJ31902L, UPC Number: 019348956435; Model Number: DYNJ31902M, UPC Number: 019532729658; Model Number: DYNJ39432I, UPC Number: 019348933454; Model Number: DYNJ39432J, UPC Number: 019532710115; Model Number: DYNJ39432K, UPC Number: 019532730509; Model Number: DYNJ41625B, UPC Number: 088994293420; Model Number: DYNJ46246A, UPC Number: 088994258496; Model Number: DYNJ53438A, UPC Number: 019348965302; Model Number: DYNJ53610C, UPC Number: 019348930032; Model Number: DYNJ53995G, UPC Number: 019532707376; Model Number: DYNJ56791A, UPC Number: 019348959411; Model Number: DYNJ56791B, UPC Number: 019532704567; Model Number: DYNJ57490A, UPC Number: 019348964199; Model Number: DYNJ58608, UPC Number: 088994287195; Model Number: DYNJ58681A, UPC Number: 088827779848; Model Number: DYNJ58681B, UPC Number: 019532729337; Model Number: DYNJ58710, UPC Number: 088994288085; Model Number: DYNJ61325A, UPC Number: 019348979445; Model Number: DYNJ61325B, UPC Number: 019532709784; Model Number: DYNJ61528, UPC Number: 019348957898; Model Number: DYNJ62399A, UPC Number: 019348925026; Model Number: DYNJ65160, UPC Number: 019348925092; Model Number: DYNJ66356, UPC Number: 019348934445; Model Number: DYNJ66356A, UPC Number: 019348983939; Model Number: DYNJ66356B, UPC Number: 019348994135; Model Number: DYNJ66356C, UPC Number: 019348999105; Model Number: DYNJ66356D, UPC Number: 019532706029; Model Number: DYNJ66577, UPC Number: 019348936096; Model Number: DYNJ68492A, UPC Number: 019348991395; Model Number: DYNJ68492B, UPC Number: 019532703330; Model Number: DYNJ68492C, UPC Number: 019532720566; Model Number: DYNJ68492D, UPC Number: 019532734221; Model…
FDA’s list runs to 7,970 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.
Barcodes and drug codes
-
UPC
019348956435 -
UPC
019348944525 -
UPC
019532715035 -
UPC
019532729658 -
UPC
019348933454 -
UPC
019532710115 -
UPC
019532730509 -
UPC
088994293420 -
UPC
088994258496 -
UPC
019348965302 -
UPC
019348930032 -
UPC
019532707376 -
UPC
019348959411 -
UPC
019532704567 -
UPC
019348964199 -
UPC
088994287195 -
UPC
088827779848 -
UPC
019532729337 -
UPC
088994288085 -
UPC
019348979445 -
UPC
019532709784 -
UPC
019348957898 -
UPC
019348925026 -
UPC
019348925092 -
UPC
019348934445 -
UPC
019348983939 -
UPC
019348994135 -
UPC
019348999105 -
UPC
019532706029 -
UPC
019348936096 -
UPC
019348991395 -
UPC
019532703330 -
UPC
019532720566 -
UPC
019532734221 -
UPC
019348984540 -
UPC
019532702645 -
UPC
019348984772 -
UPC
019532705334 -
UPC
019532712706 -
UPC
019532716359 -
UPC
019532717108 -
UPC
019532717803 -
UPC
019532720722 -
UPC
019532735023 -
UPC
019532723568 -
UPC
019348959858 -
UPC
019348969592 -
UPC
088827776727 -
UPC
019532703914 -
UPC
088994270504 -
UPC
019532717634 -
UPC
019348983069 -
UPC
019532708884 -
UPC
019348987387 -
UPC
019348992622 -
UPC
019532733085 -
UPC
019532734322 -
UPC
019348942486 -
UPC
019348938687 -
UPC
019348996690 -
UPC
019532712350 -
UPC
019348931287 -
UPC
088994268907 -
UPC
019532720900 -
UPC
019348922643 -
UPC
019348995136 -
UPC
019532721211 -
UPC
088994229774 -
UPC
019348949439 -
UPC
019532701580 -
UPC
019348969667 -
UPC
019348981050 -
UPC
088827789060 -
UPC
088994224214 -
UPC
019348983731 -
UPC
019348966323 -
UPC
019348969283 -
UPC
019348943314 -
UPC
019348935171 -
UPC
088994271048 -
UPC
019348979335 -
UPC
019348939718 -
UPC
088994212841 -
UPC
088438979693 -
UPC
088827759997 -
UPC
088994252942 -
UPC
088994210530 -
UPC
088994223706 -
UPC
019348936103 -
UPC
088994238558 -
UPC
019348974565 -
UPC
088994271442 -
UPC
088994253967 -
UPC
019348928316 -
UPC
088994272740 -
UPC
088994268001 -
UPC
088994266543 -
UPC
088994282388 -
UPC
019348946631 -
UPC
088994274827 -
UPC
088994278233 -
UPC
088994279429 -
UPC
088994281667 -
UPC
088994287126 -
UPC
019348948756 -
UPC
019348943433 -
UPC
019532703087 -
UPC
019348961635 -
UPC
019348946987 -
UPC
019348949512 -
UPC
019348976342 -
UPC
019348979637 -
UPC
019348941415 -
UPC
019348928038 -
UPC
019348931778 -
UPC
019348943555 -
UPC
019348983668 -
UPC
019348988372 -
UPC
019532704086 -
UPC
019532708820 -
UPC
019532708250 -
UPC
019532723550 -
UPC
019348935468 -
UPC
019348981468 -
UPC
019532709850 -
UPC
019348936966 -
UPC
019348943849 -
UPC
019348932240 -
UPC
019348923016 -
UPC
088994268856 -
UPC
088994270310 -
UPC
019348930662 -
UPC
088994293861 -
UPC
019348930714 -
UPC
019348948263 -
UPC
019532726779 -
UPC
019348986248 -
UPC
019348931923 -
UPC
019348935608 -
UPC
019532720495
As FDA’s description and codes give them; the UPCs written as digits only.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide distribution - US Nationwide and the countries of Canada, China, Costa Rica, India, Lebanon, Panama, Qatar, Saudi Arabia, Singapore, United Arab Emirates.
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 May 15, 2023.
- FDA classified it on Aug 3, 2023.
- FDA’s Enforcement Report published it on Aug 9, 2023.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- MEDLINE INDUSTRIES, LP - Northfield, of Northfield, IL.
- 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 7,970 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.