Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.
This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone. Most recalls are Class II or III.
Medline Convenience kits labeled as: 1) PSP - VAMC LONG BEACH, Pack Number 146255; 2) INSERTION TRAY, Pack Number CVI5080; 3) INCISION & DRAINAGE TRAY, Pack Number DYNDA1063; 4) DRAINAGE ACCESS PACK 319701 , Pack Number DYNJ44599I ; 5) PROCEDURE DRAINAGE KIT, Pack Number DYNJ66416; 6) DRAINAGE TRAY , Pack Number DYNJ68767; 7) INCISION AND DRAINAGE TRAY, Pack Number P737057
Why it was recalled
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.
Is your unit affected?
The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.
A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.
Show the FDA's listed lot / code information
146255, Lot Number 23KBP730; 146255, Lot Number 23JBV770; 146255, Lot Number 23BBJ516; 146255, Lot Number 23ABS205; 146255, Lot Number 22LBQ260; 146255, Lot Number 22LBF150; CVI5080, Lot Number 24ABR654 ; CVI5080, Lot Number 24ABS414 ; DYNDA1063, Lot Number 21JBR507 ; DYNJ44599I , Lot Number 21FBO112 ; DYNJ44599I , Lot Number 21GBQ754 ; DYNJ44599I , Lot Number 21HBU200 ; DYNJ44599I , Lot Number 21KBM267 ; DYNJ44599I , Lot Number 21LBQ208 ; DYNJ44599I , Lot Number 22NBE952 ; DYNJ44599I , Lot Number 22EBA808 ; DYNJ44599I , Lot Number 22EBV387 ; DYNJ44599I , Lot Number 22GBL830 ; DYNJ44599I , Lot Number 22HBM625 ; DYNJ44599I , Lot Number 22IBN180 ; DYNJ44599I , Lot Number 22JBH998 ; DYNJ44599I , Lot Number 22JBX287 ; DYNJ44599I , Lot Number 23ABJ748 ; DYNJ44599I , Lot Number 23BBO863 ; DYNJ44599I , Lot Number 23CBU289 ; DYNJ44599I , Lot Number 23DBO841 ; DYNJ44599I , Lot Number 23EBP969 ; DYNJ44599I , Lot Number 23GBG623 ; DYNJ44599I , Lot Number 23HBR164 ; DYNJ44599I , Lot Number 20EBC852 ; DYNJ44599I , Lot Number 23IBU633 ; DYNJ44599I , Lot Number 20FBO439 ; DYNJ44599I , Lot Number 20GBA511 ; DYNJ44599I , Lot Number 23KBI875 ; DYNJ44599I , Lot Number 24ABA732 ; DYNJ44599I , Lot Number 20JBA956 ; DYNJ44599I , Lot Number 20JBZ002 ; DYNJ44599I , Lot Number 20KBD800 ; DYNJ44599I , Lot Number 20LBI387 ; DYNJ44599I , Lot Number 21CBN891 ; DYNJ44599I , Lot Number 21CBX162 ; DYNJ66416, Lot Number 20GKA807 ; DYNJ68767, Lot Number 21HLA622 ; DYNJ68767, Lot Number 21KLA137 ; DYNJ68767, Lot Number 21LLA666 ; DYNJ68767, Lot Number 22BLA542 ; DYNJ68767, Lot Number 22DLB131 ; DYNJ68767, Lot Number 22HLA449 ; DYNJ68767, Lot Number 22ILA208 ; DYNJ68767, Lot Number 22KLA881 ; DYNJ68767, Lot Number 23ALA469 ; DYNJ68767, Lot Number 23BLA292 ; DYNJ68767, Lot Number 23CLA817 ; DYNJ68767, Lot Number 23ELA407 ; DYNJ68767, Lot Number 23ELA587 ; DYNJ68767, Lot Number 23KLA248 ; DYNJ68767, Lot Number 23LLA473 ; P737057, Lot Number 21VBC482
Recall status
Ongoing — the recall is still being carried out.
Where it was distributed
Worldwide distribution.
Recall record
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Product type
- Devices
- Recall number
- Z-3015-2024
- Voluntary / mandated
- Voluntary: Firm initiated
- Initial notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Origin
- Northfield, IL
- Recall initiated
- 2024-04-08
What to do
Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.
Also available: structured data (JSON-LD) · recall record (JSON)
What this is — and is not
A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.
To report a problem you experienced, use
FDA MedWatch.
Verify this record at FDA recalls ·
Recall Z-3015-2024 · Source: openFDA enforcement.