Medline Convenience kits labeled as: 1) URETEROSCOPY CDS SC-LF, Pack Number CDS983922F
Medical device recall Z-3005-2024. 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) URETEROSCOPY CDS SC-LF, Pack Number CDS983922F ; 2) URETEROSCOPY TRAY-RF, Pack Number DYNJ27442U ; 3) URETHROPLASTY PACK, Pack Number DYNJ39700B ; 4) RRP PACK, Pack Number DYNJ44109B ; 5) PROSTATECTOMY PACK-LF , Pack Number DYNJ66109A ; 6) PERINEAL PACK , Pack Number DYNJ69895; 7) LIVER 2018, Pack Number DYNJ905655A; 8) UROLOGY PACK, Pack Number DYNJT2255M
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
CDS983922F , Lot Number 19BDC122 ; CDS983922F , Lot Number 19CDC327 ; CDS983922F , Lot Number 19EDB619 ; CDS983922F , Lot Number 19HDB982 ; CDS983922F , Lot Number 19JDA589 ; CDS983922F , Lot Number 19JDC196 ; CDS983922F , Lot Number…
Every code shown here, 1,741 characters
CDS983922F , Lot Number 19BDC122 ; CDS983922F , Lot Number 19CDC327 ; CDS983922F , Lot Number 19EDB619 ; CDS983922F , Lot Number 19HDB982 ; CDS983922F , Lot Number 19JDA589 ; CDS983922F , Lot Number 19JDC196 ; CDS983922F , Lot Number 20DDB450 ; CDS983922F , Lot Number 20FDB626 ; CDS983922F , Lot Number 20GDA441 ; CDS983922F , Lot Number 20HDA774 ; CDS983922F , Lot Number 20IDA727 ; CDS983922F , Lot Number 20JDC665 ; CDS983922F , Lot Number 21DDB315 ; DYNJ27442U , Lot Number 21HBM391 ; DYNJ27442U , Lot Number 21KBS771 ; DYNJ27442U , Lot Number 21LBY698 ; DYNJ39700B , Lot Number 20CBK667 ; DYNJ39700B , Lot Number 20DBC549 ; DYNJ39700B , Lot Number 20IMA568 ; DYNJ39700B , Lot Number 20KMA519 ; DYNJ39700B , Lot Number 20LME505 ; DYNJ39700B , Lot Number 21DMD882 ; DYNJ39700B , Lot Number 21FMC569 ; DYNJ39700B , Lot Number 21FMF531 ; DYNJ39700B , Lot Number 21GMF302 ; DYNJ39700B , Lot Number 21HMD242 ; DYNJ39700B , Lot Number 21JMH252 ; DYNJ39700B , Lot Number 21KMF491 ; DYNJ39700B , Lot Number 22AMG337 ; DYNJ44109B , Lot Number 21IMF271 ; DYNJ44109B , Lot Number 21JMD783 ; DYNJ44109B , Lot Number 21KME283 ; DYNJ66109A , Lot Number 21JBN809 ; DYNJ66109A , Lot Number 21KBC511 ; DYNJ66109A , Lot Number 22CBP867 ; DYNJ69895, Lot Number 21KBU119 ; DYNJ69895, Lot Number 22EBD392 ; DYNJ69895, Lot Number 22GBH506 ; DYNJ905655A, Lot Number 21ILA013 ; DYNJ905655A, Lot Number 21ILA926 ; DYNJ905655A, Lot Number 21JLB171 ; DYNJ905655A, Lot Number 22ALA375 ; DYNJ905655A, Lot Number 22BLA544 ; DYNJ905655A, Lot Number 22CLB377 ; DYNJ905655A, Lot Number 22ELA391 ; DYNJT2255M , Lot Number 21IMF282 ; DYNJT2255M , Lot Number 21JMC072 ; DYNJT2255M , Lot Number 21JMI117 ; DYNJT2255M , Lot Number 21KMF688 ; DYNJT2255M , Lot Number 21KMG176
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.”
- 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.