Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel
Medical device recall Z-2319-2023. 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
- 83,541 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. 7F, 20CM TRIPLE LUMEN CVC BUNDLE, Model Number: ECVC4740; b. A V GRAFT, Model Number: DYNJ36212C; c. AAA, Model Number: DYNJ905651, DYNJ905651A, DYNJ905651B; d. AAA PACK, Model Number: DYNJ44918C; e. AAA PACK - TEAM 3, Model Number: DYNJ44847G; f. ABLATION PACK, Model Number: DYNJ62540, DYNJ64068; g. ABLATION/DRAINAGE PACK, Model Number: DYNJ53658A; h. ACCESS KIT, Model Number: DYNDH1159A; i. ACCESS PACK, Model Number: DYNJ69017; j. ACCESSORY KIT, Model Number: DYNJ901348D; k. ADULT CORONARY PACK, Model Number: DYNJV0275F; l. ADULT CVC MAX BARRIER KIT-LF, Model Number: DYNJ38714B; m. ALL PURPOSE TRAY FOAKS, Model Number: DYNJ63576, DYNJ63576A; n. AMINO KIT; Model Number: DYNDH1649; o. AMNIOCENTESIS TRAY, Model Number: DYNDH1420; p. ANGIO STANDARD PACK-LF, Model Number: DYNJ0370436Q; q. ANGIO TRAY, Model Number: DYNJ23438J; r. ANGIOGRAM PACK, Model Number: DYNJ47004B; s. ANGIOGRAM TRAY, Model Number: DYNJ33638I; t. ANGIO-VASCULAR, Model Number: DYNJ24272B; u. ARTERIAL PACK, Model Number: DYNJ51340D; v. ARTERIO-VENOUS CDS, Model Number: CDS984186C; w. ASPIRATION TRAY, Model Number: DYNDH1467; x. ASPIRE EXACT TRAY, Model Number: DYNJRA1716, DYNJRA1716A; y. BARIATRIC LAPAROSCOPY R-Y PACK, Model Number: DYNJC9299L; z. BASIC PACK, Model Number: DYNJ37460A, DYNJ42691, DYNJ52122B, DYNJ52171, DYNJ55456, DYNJ55457, DYNJ81343; aa. BASIC PROCEDURE PACK, Model Number: DYNJ53122B; bb. BASIC VEIN PACK, Model Number: DYNJ58650; cc. BEDSIDE PROCEDURE PREP KIT, Model Number: MNS7695A; dd. BGMC LIVER TRANSPLANT, Model Number: DYNJ9664651D; ee. BIOPSY TRAY, Model Number: DYNDH1340; ff. BLOCK KIT, Model Number: DYNJRA1145; gg. BLOCK SUPPLIES NDL CNTR, Model Number: DYNJRA1755; hh. BREAST ULTRASOUND PROCEDURE TR, Model Number: DYNDL1596A; ii. BUNDLE KIT, Model Number: DYNJ49737B, DYNJ49737C; jj. C V MAJOR PACK, Model Number: DYNJ64861; kk. CABG UNIVERSITY HOSP PACK-LF, Model Number: DYNJ0375705L; ll. CAROTID ENDARTERECTOMY, Model Number: DYNJ905640; mm. CHEST TUBE INSERTION TRAY, Model Number: TRICHT1120; nn. CHP TRANSPLANT CDS, Model Number: CDS983082I, CDS983082J; oo. CLINIC PACK, Model Number: DYNJRA1578; pp. CLOSURE CDS, Model Number: CDS983704G, CDS983704I; qq. CLOSURE FAST PACK UNIV, Model Number: DYNJ53482A; rr. CLOSURE PACK, Model Number: DYNJ54437A, DYNJ54437C, DYNJ57514, DYNJ60804; ss. CLOSURE PACK-LF, Model Number: DYNJ0807503M; tt. CLOSURE PROCEDURE, Model Number: DYNJ59206; uu. CLOSURE PROCEDURE PACK, Model Number: DYNJ66741; vv. CLOSURE PROCEDURE PKSJO-LF, Model Number: DYNJ35409F; ww. CLOT RETRIEVAL PACK, Model Number: DYNJ56140B; xx. CLOVIS MINOR IR PROCEDURE-LF, Model Number: DYNJ61067; yy. COMMANDO PACK MSH-LF, Model Number: DYNJ48525D; zz. CONTINUOUS BLOCK, Model Number: DYNJRA0960B; aaa. COPS PROCEDURE PACK-LF, Model Number: DYNJ68923A; bbb. CRMC MINOR IR PROCEDURE PK-LF, Model Number: DYNJ61099, DYNJ61099A; ccc. CV AAA PACK W AUX, Model Number: DYNJ65710; ddd. CV ACCESS PACK WRO-LF, Model Number: DYNJ41875B; eee. CV CDS, Model Number: CDS985395C; fff. CV MINOR CDS, Model Number: CDS984100T; ggg. CV PACK, Model Number: DYNJ45074B; hhh. CVC PACK, Model Number: DYNJ44010; iii. CVL PACK, Model Number: DYNJ00281N; jjj. CVOR CDS-LF, Model Number: CDS840198V; kkk. CYSTO PACK SMGH-LF, Model Number: DYNJ41915A; lll. DAVIES PHALLOPLASTY PACK, Model Number: DYNJ52185F; mmm. DAVINCI, Model Number: DYNJ906543A; nnn. DBD-BASIC PACK, Model Number: DYNJ55458; ooo. DBD-BIOPSY PACK-LF, Model Number: DYNJ0747885F; ppp. DBD-DONOR FREE FLAP PACK-LF, Model Number: DYNJ0426069M; qqq. DBD-ECMO MODULE PACK, Model Number: DYNJ55669F; rrr. DBD-EVLA PACK, Model Number: DYNJ6
83,541 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: ECVC4740, UPC Number: 10653160335214. b. Model Number: DYNJ36212C, UPC Number: 088994288566. c.…
Every code shown here, 1,996 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: ECVC4740, UPC Number: 10653160335214. b. Model Number: DYNJ36212C, UPC Number: 088994288566. c. Model Number: DYNJ905651, UPC Number: 088827778831; Model Number: DYNJ905651A, UPC Number: 019348968651; Model Number: DYNJ905651B, UPC Number: 019348992506. d. Model Number: DYNJ44918C, UPC Number: 019348976679. e. Model Number: DYNJ44847G, UPC Number: 019348962983. f. Model Number: DYNJ62540, UPC Number: 019348966647; Model Number: DYNJ64068, UPC Number: 019348978313. g. Model Number: DYNJ53658A, UPC Number: 088994268440. h. Model Number: DYNDH1159A, UPC Number: 088994288165. i. Model Number: DYNJ69017, UPC Number: 019348987815. j. Model Number: DYNJ901348D, UPC Number: 019348959468. k. Model Number: DYNJV0275F, UPC Number: 019348926312. l. Model Number: DYNJ38714B, UPC Number: 088994260193. m. Model Number: DYNJ63576, UPC Number: 019348976954; Model Number: DYNJ63576A, UPC Number: 019348942925. n. Model Number: DYNDH1649, UPC Number: 019348994436. o. Model Number: DYNDH1420, UPC Number: 019348936044. p. Model Number: DYNJ0370436Q, UPC Number: 088827777928. q. Model Number: DYNJ23438J, UPC Number: 019348956435. r. Model Number: DYNJ47004B, UPC Number: 088827775429. s. Model Number: DYNJ33638I, UPC Number: 019348956435. t. Model Number: DYNJ24272B, UPC Number: 019348956435. u. Model Number: DYNJ51340D, UPC Number: 019348956981. v. Model Number: CDS984186C, UPC Number: 088994295750. w. Model Number: DYNDH1467, UPC Number: 019348943966. x. Model Number: DYNJRA1716, UPC Number: 019348926312; Model Number: DYNJRA1716A, UPC Number: 019348989641. y. Model Number: DYNJC9299L, UPC Number: 019348926312. z. Model Number: DYNJ37460A, UPC Number: 088827756043; Model Number: DYNJ42691, UPC Number: 088827700350; Model Number: DYNJ52122B, UPC Number: 019348993530; Model Number: DYNJ52171, UPC Number: 088994224347; Model Number: DYNJ55456, UPC…
FDA’s list runs to 7,084 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
10653160335214 -
UPC
088994288566 -
UPC
088827778831 -
UPC
019348968651 -
UPC
019348992506 -
UPC
019348976679 -
UPC
019348962983 -
UPC
019348966647 -
UPC
019348978313 -
UPC
088994268440 -
UPC
088994288165 -
UPC
019348987815 -
UPC
019348959468 -
UPC
019348926312 -
UPC
088994260193 -
UPC
019348976954 -
UPC
019348942925 -
UPC
019348994436 -
UPC
019348936044 -
UPC
088827777928 -
UPC
019348956435 -
UPC
088827775429 -
UPC
019348956981 -
UPC
088994295750 -
UPC
019348943966 -
UPC
019348989641 -
UPC
088827756043 -
UPC
088827700350 -
UPC
019348993530 -
UPC
088994224347 -
UPC
088994254844 -
UPC
088994254846 -
UPC
019532711306 -
UPC
019348932122 -
UPC
088994287665 -
UPC
065316034345 -
UPC
019348939642 -
UPC
088994289450 -
UPC
088994292854 -
UPC
019348984284 -
UPC
088438992650 -
UPC
019348939440 -
UPC
019532723588 -
UPC
019348922377 -
UPC
019348954413 -
UPC
019348952767 -
UPC
065316031829 -
UPC
088994277286 -
UPC
019348967451 -
UPC
019348927278 -
UPC
088994280844 -
UPC
019348985455 -
UPC
088994291731 -
UPC
088994256796 -
UPC
019348924397 -
UPC
088994274784 -
UPC
019348953278 -
UPC
088994209173 -
UPC
088827776557 -
UPC
019348937494 -
UPC
088827777124 -
UPC
019348954767 -
UPC
019348954222 -
UPC
019348975077 -
UPC
019532707079 -
UPC
019348954424 -
UPC
019348946396 -
UPC
019348928508 -
UPC
019348956307 -
UPC
088994286348 -
UPC
019348939994 -
UPC
088994284064 -
UPC
088827707945 -
UPC
088994295567 -
UPC
088827756881 -
UPC
019348936871 -
UPC
019348981803 -
UPC
088994254845 -
UPC
019532720575 -
UPC
019532731371 -
UPC
019532719423 -
UPC
019348991424 -
UPC
088994272434 -
UPC
019348983968 -
UPC
019348925174 -
UPC
019348942281 -
UPC
019348997120 -
UPC
088994219386 -
UPC
088994282864 -
UPC
019348945716 -
UPC
019348985856 -
UPC
088994286535 -
UPC
088994286537 -
UPC
019348991717 -
UPC
019532717136 -
UPC
088994253675 -
UPC
019348986686 -
UPC
088827759528 -
UPC
019348954451 -
UPC
019348938641 -
UPC
019532707150 -
UPC
019348953302 -
UPC
088827773629 -
UPC
088827758069 -
UPC
019532726659 -
UPC
019348958721 -
UPC
019348939016 -
UPC
019348920588 -
UPC
019348987734 -
UPC
019348985231 -
UPC
019348935382 -
UPC
019532719811 -
UPC
019348956964 -
UPC
019348940904 -
UPC
019348949583 -
UPC
088994205905
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 7,084 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.