Medline Convenience kits labeled as: 1) KIT GENERAL CLOSURE , Pack Number DYKMBNDL200A
Medical device recall Z-3028-2024. Published in FDA’s Enforcement Report on Sep 18, 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 18, 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?
Medline Convenience kits labeled as: 1) KIT GENERAL CLOSURE , Pack Number DYKMBNDL200A ; 2) KIT GENERAL CLOSURE , Pack Number DYKMBNDL200AH; 3) CUST CHEST TUBE INSERTION X , Pack Number DYNDA2415B ; 4) LACERATION TRAY , Pack Number DYNDL1495A ; 5) LACERATION TRAY , Pack Number DYNDL1495AH; 6) LACERATION TRAY , Pack Number DYNDL1807B ; 7) LACERATION WITH INSTMTS TRAY, Pack Number DYNDL1963; 8) LACERATION WITH INSTMTS TRAY, Pack Number DYNDL1963H ; 9) LACERATION TRAY , Pack Number DYNDL1965A ; 10) STERILE RESUTURE PACK, Pack Number DYNDL1980A; 11) STERILE RESUTURE PACK, Pack Number DYNDL1980AH; 12) LACERATION TRAY , Pack Number DYNDL1981; 13) LACERATION TRAY , Pack Number DYNDL1985; 14) SUTURE TRAY , Pack Number DYNDL1986; 15) FGH FLOOR KIT , Pack Number DYNDL1989; 16) LACERATION KIT, Pack Number DYNDL1991; 17) LACERATION KIT, Pack Number DYNDL1992; 18) LACERATION KIT, Pack Number DYNDL1992H ; 19) ER LACERATION TRAY, Pack Number DYNDL1993; 20) LACERATION TRAY , Pack Number DYNDL1994; 21) CLOSURE PACK-LF , Pack Number DYNJ0807503N ; 22) CLOSING BUNDLE, Pack Number DYNJ52157I ; 23) PREMIUM CLOSUREPLUS PACK, Pack Number DYNJ54326A ; 24) ABD CLOSURE PACK, Pack Number DYNJ56987C ; 25) CLOSING PACK, Pack Number DYNJ57577A ; 26) SURGERY CLOSING KIT , Pack Number DYNJ67429B ; 27) CLOSING PACK, Pack Number DYNJ68267B ; 28) MICRODISECTOMY PACK , Pack Number DYNJ80585B ; 29) PREP TRAY , Pack Number DYNJRA1583D; 30) NECESSAIRES A POINT DE SUTURES, Pack Number M101498; 31) MAJOR LACERATION PACK-LF, Pack Number PHS751688G; 32) IR SUTURE PACK-LF , Pack Number PHS863717D ; 33) FINE LACERATION KIT , Pack Number SUT17215A; 34) MINOR LACERATION TRAY , Pack Number SUT18200 ; 35) LACERATION TRAY, Pack Number SUT20285A; 36) LACERATION TRAY W/ LIDOCAINE, Pack Number SUT20595A; 37) SNAG FREE LACERATION TRAY, Pack Number SUT21665; 38) LACERATION TRAY , Pack Number SUT21710 ; 39) LACERATION REPAIR TRAY, Pack Number SUT21780 ; 40) SNAG FREE LACERATION TRAY , Pack Number SUT21825
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
DYKMBNDL200A , Lot Number 22KBD675 ; DYKMBNDL200A , Lot Number 23KBA331 ; DYKMBNDL200AH, Lot Number 22KBD675 ; DYKMBNDL200AH, Lot Number 23KBA331 ; DYNDA2415B , Lot Number 23JLA114 ; DYNDA2415B , Lot Number 24BLB045 ; DYNDL1495A , Lot…
Every code shown here, 1,995 characters
DYKMBNDL200A , Lot Number 22KBD675 ; DYKMBNDL200A , Lot Number 23KBA331 ; DYKMBNDL200AH, Lot Number 22KBD675 ; DYKMBNDL200AH, Lot Number 23KBA331 ; DYNDA2415B , Lot Number 23JLA114 ; DYNDA2415B , Lot Number 24BLB045 ; DYNDL1495A , Lot Number 22LBJ768 ; DYNDL1495A , Lot Number 23ABG899 ; DYNDL1495A , Lot Number 23CBF146 ; DYNDL1495A , Lot Number 23DBO301 ; DYNDL1495A , Lot Number 23EBC524 ; DYNDL1495A , Lot Number 23EBR564 ; DYNDL1495A , Lot Number 23GBC601 ; DYNDL1495A , Lot Number 23HBF407 ; DYNDL1495A , Lot Number 23IBR368 ; DYNDL1495A , Lot Number 23KBF026 ; DYNDL1495AH, Lot Number 22LBJ768 ; DYNDL1495AH, Lot Number 23ABG899 ; DYNDL1495AH, Lot Number 23CBF146 ; DYNDL1495AH, Lot Number 23DBO301 ; DYNDL1495AH, Lot Number 23EBC524 ; DYNDL1495AH, Lot Number 23EBR564 ; DYNDL1495AH, Lot Number 23GBC601 ; DYNDL1495AH, Lot Number 23HBF407 ; DYNDL1495AH, Lot Number 23IBR368 ; DYNDL1495AH, Lot Number 23KBF026 ; DYNDL1807B , Lot Number 21JBR532 ; DYNDL1963, Lot Number 22JMG284 ; DYNDL1963H , Lot Number 22JMG284 ; DYNDL1965A , Lot Number 21JBJ528 ; DYNDL1980A, Lot Number 23KBE409; DYNDL1980AH, Lot Number 23KBE409; DYNDL1981, Lot Number 22GBU753 ; DYNDL1981, Lot Number 22LBS274 ; DYNDL1981, Lot Number 23ABL575 ; DYNDL1981, Lot Number 23BBJ949 ; DYNDL1981, Lot Number 23CBG983 ; DYNDL1985, Lot Number 22JBN831 ; DYNDL1985, Lot Number 23CBQ478 ; DYNDL1985, Lot Number 23DBF367 ; DYNDL1986, Lot Number 22LBJ084 ; DYNDL1986, Lot Number 23FBO474 ; DYNDL1986, Lot Number 23GBE045 ; DYNDL1989, Lot Number 23DBN197 ; DYNDL1989, Lot Number 23FBB552 ; DYNDL1989, Lot Number 23GBR197 ; DYNDL1991, Lot Number 23IMG395 ; DYNDL1992, Lot Number 23IBH341 ; DYNDL1992, Lot Number 23KBA670 ; DYNDL1992H , Lot Number 23IBH341 ; DYNDL1992H , Lot Number 23KBA670 ; DYNDL1993, Lot Number 23JBP617 ; DYNDL1994, Lot Number 23KBF825 ; DYNDL1994, Lot Number 23LBV214 ; DYNJ0807503N , Lot Number 23FME235 ; DYNJ52157I , Lot Number 23EBQ422 ; DYNJ52157I , Lot Number 23FBO768 ; DYNJ52157I , Lot Number 23HBG369 ;…
FDA’s list runs to 4,998 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 distribution.
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 Sep 6, 2024.
- FDA’s Enforcement Report published it on Sep 18, 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 4,998 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.