Centurion procedure kits labeled as: 1) 3” RADIAL ARTERIAL LINE KIT- ICU, Pack Number ART240B
Medical device recall Z-2768-2024. Published in FDA’s Enforcement Report on Sep 4, 2024.
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 Sep 4, 2024. Copied from openFDA on Oct 20, 2026.
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?
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Centurion procedure kits labeled as: 1) 3” RADIAL ARTERIAL LINE KIT- ICU, Pack Number ART240B; 2) 5FR 2L PICC LINE TRAY, Pack Number PICC0020; 3) 6” FEMORAL ARTERIAL LINE KIT, Pack Number ART245B; 4) ADVANCED REPAIR KIT, Pack Number SUT15940; 5) ARTHROGRAM TRAY, Pack Number SPEC0004C; 6) ARTHROGRAM TRAY, Pack Number DYNDH1134; 7) ARTHROGRAM TRAY-LF, Pack Number SPEC0400; 8) ARTHROGRAM/LP/MYELOGRAM TRAY, Pack Number PT220; 9) AULTMAN HOSPITAL CHEST TUBE INSERTION TR, Pack Number CHT500; 10) BIOPSY BASIC PACK, Pack Number P784604; 11) BIOPSY KIT, Pack Number DYNDA1466A; 12) BIOPSY SKIN/LACERATION TRAY, Pack Number SUT20455; 13) BIOPSY TRAY, Pack Number BT1015; 14) BIOPSY TRAY, Pack Number DYNDH1273; 15) BIOPSY TRAY, Pack Number BT1060; 16) BIOPSY TRAY, Pack Number DYNDH1340; 17) BIOPSY TRAY, Pack Number P151659; 18) BIOPSY TRAY, Pack Number SPEC0292; 19) BIOPSY TRAY, Pack Number DYNDH1314A; 20) BIOPSY TRAY, Pack Number DYNDH1137C; 21) BIOPSY TRAY - LF, Pack Number DYNJTS0018A; 22) BIOPSY TRAY-LF, Pack Number SPEC4380; 23) BIOPSY/ARTHROGRAM TRAY, Pack Number DYNDH1115; 24) BONE MARROW BIOPSY ASPIRATION, Pack Number DYNJTS0214; 25) BREAST BIOPSY TRAY, Pack Number SPEC0130C; 26) CATHETER ON/OFF KIT, Pack Number DT5490B; 27) CDP, INTRODUCER KIT 9F, Pack Number S5078BF09; 28) CHEST TUBE INSERTION TRAY, Pack Number CHT705; 29) CHEST TUBE INSERTION TRAY, Pack Number CHT1900; 30) CHEST TUBE, UMBI LINE PK, Pack Number DYNDA1432A; 31) CIRCUMCISION TRAY, Pack Number CIT6260; 32) CIRCUMCISION/MINOR TRAY, Pack Number CIT6785A; 33) CONGENITAL ADD-ON KIT, Pack Number DYNDA2213A; 34) CORE BIOPSY TRAY, Pack Number SPEC0083B; 35) CT BIOPSY TRAY W/CHLORAPREP, Pack Number DYNJ05162; 36) CUSTOM BIOPSY TRAY, Pack Number MNS4815; 37) CUSTOM BX TRAY, Pack Number SPEC0071B; 38) DELIVERY ACCESSORY KIT, Pack Number MNS6496; 39) DIAGNOSTIC TRAY, Pack Number DYNDH1359; 40) E. R. LACERATION TRAY, Pack Number DYNDL1187A; 41) ER CHEST TUBE TRAY, Pack Number CHT1570A; 42) ER LACERATION TRAY C WEST, Pack Number DYNDL2952; 43) FACET BLOCK TRAY-AVERY MELVIN, Pack Number DYNJRA0421; 44) FINE LACERATION KIT, Pack Number SUT19360; 45) FINE LACERATION KIT, Pack Number SUT17215; 46) HH PACK BIOPSY, Pack Number BT345; 47) HSG TRAY, Pack Number DYNDH1453; 48) I&D TRAY, Pack Number ID2165; 49) INCISION & DRAINAGE TRAY, Pack Number ID2060; 50) INFECTION DRIVELINE MANAGEMENT KIT, Pack Number DM645; 51) I-PACK INJECTION KIT WITH DRAPE, Pack Number MNS12150; 52) ISHAK I.R. BIOPSY TRAY, Pack Number DYNDH1297; 53) LACERATION TRAY, Pack Number SUT20955; 54) LACERATION TRAY, Pack Number DYNDL1772; 55) LACERATION TRAY, Pack Number DYNDL1250C; 56) LACERATION TRAY, Pack Number DYNDL1887; 57) LACERATION TRAY, Pack Number SUT3780; 58) LACERATION TRAY, Pack Number DYNDL1774A; 59) LACERATION TRAY, Pack Number SUT18080; 60) LACERATION TRAY, Pack Number SUT21490; 61) LOCAL INFILTRATION TRAY, Pack Number DYNDH1406; 62) LUMBAR EPIDURAL TRAY-LF, Pack Number DYNJRA0313B; 63) LUMBAR PUNCTURE TRAY, Pack Number DYNDH1321; 64) LUMBAR PUNCTURE TRAY, Pack Number SPEC0289; 65) LUMBAR PUNCTURE TRAY, Pack Number PT215; 66) LUMBAR TRAY, Pack Number SPEC0177; 67) LUMBAR TRAY, Pack Number DYNDH1540A; 68) MAMMOGRAPHY BIOPSY TRAY, Pack Number DYNDH1304A; 69) MINI INTERVENTIONAL PACK, Pack Number DYNDH1324; 70) MYELO / ARTHRO TRAY, Pack Number DYNDH1332A; 71) MYELOGRAM TRAY, Pack Number DYNJTS0516A; 72) MYELOGRAM TRAY, Pack Number DYNJTS0514; 73) MYELOGRAM TRAY, Pack Number DYNDH1531; 74) OB DELIVERY SET, Pack Number MNS3355; 75) OB DELIVERY TRAY, Pack Number MNS5575; 76) OHS CT BIOPSY TRAY -LF, Pack Number DYNDH1270; 77) ONCOLOGY-HEMOTOLOGY PREP TRAY-STERILE/LF, Pack Number DYNDA2523; 78) PACEMAKER TRAY, Pack Number MNS12700; 79) PACEMAKER TRAY, Pack Number MNS12625; 80) PACEMAKER TRAY, Pack Number MNS12700A; 81) PACK,CHALAZION SEY59CHCHA, Pack Number DYNDL1571B; 82) PEDI ULTRASOUND GUIDED PIV KIT, Pack Number IVS3320; 83)
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
ART240B, Lot Number 2023083190; PICC0020, Lot Number 2023122290; ART245B, Lot Number 2023020990; ART245B, Lot Number 2023071090; SUT15940, Lot Number 2021070290; SUT15940, Lot Number 2022090190; SUT15940, Lot Number 2022092690; SPEC0004C,…
Every code shown here, 1,999 characters
ART240B, Lot Number 2023083190; PICC0020, Lot Number 2023122290; ART245B, Lot Number 2023020990; ART245B, Lot Number 2023071090; SUT15940, Lot Number 2021070290; SUT15940, Lot Number 2022090190; SUT15940, Lot Number 2022092690; SPEC0004C, Lot Number 2019042990; DYNDH1134, Lot Number 2020032050; SPEC0400, Lot Number 2021120990; SPEC0400, Lot Number 2022090190; SPEC0400, Lot Number 2023050390; PT220, Lot Number 2018082290; PT220, Lot Number 2020040890; PT220, Lot Number 2020051490; PT220, Lot Number 2020061090; PT220, Lot Number 2020071590; PT220, Lot Number 2020122190; PT220, Lot Number 2021040790; PT220, Lot Number 2021050390; PT220, Lot Number 2021080690; PT220, Lot Number 2021082790; PT220, Lot Number 2021100690; PT220, Lot Number 2022082490; PT220, Lot Number 2023030290; PT220, Lot Number 2023110690; PT220, Lot Number 2023122290; PT220, Lot Number 2024031190; CHT500, Lot Number 2021113090; CHT500, Lot Number 2021121690; CHT500, Lot Number 2022050390; CHT500, Lot Number 2023060190; CHT500, Lot Number 2023070390; CHT500, Lot Number 2023092290; P784604, Lot Number 2019081980; DYNDA1466A, Lot Number 2022092690; SUT20455, Lot Number 2018090690; SUT20455, Lot Number 2019022590; SUT20455, Lot Number 2019042990; SUT20455, Lot Number 2019101690; SUT20455, Lot Number 2019112590; SUT20455, Lot Number 2020040690; SUT20455, Lot Number 2021042190; SUT20455, Lot Number 2021062590; SUT20455, Lot Number 2021081090; SUT20455, Lot Number 2022070590; SUT20455, Lot Number 2023070590; SUT20455, Lot Number 2023100590; SUT20455, Lot Number 2023122990; BT1015, Lot Number 2019013190; DYNDH1273, Lot Number 2019080190; BT1060, Lot Number 2019091090; DYNDH1340, Lot Number 2019100190; BT1060, Lot Number 2019103190; P151659, Lot Number 2019112590; DYNDH1340, Lot Number 2019121290; SPEC0292, Lot Number 2020012290; BT1015, Lot Number 2020082490; BT1060, Lot Number 2020082890; DYNDH1314A, Lot Number 2020100901; BT1015, Lot Number 2020102990; DYNDH1137C, Lot Number 2020102990; BT1015, Lot Number…
FDA’s list runs to 11,229 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.
worldwide
These words name no state.
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
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 8, 2024.
- FDA classified it on Aug 28, 2024.
- FDA’s Enforcement Report published it on Sep 4, 2024.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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 11,229 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.