Reported Sep 9, 2026 · Ongoing · Updated Sep 14, 2026
Medline Convenience Kits
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline Convenience Kits
53 of 53 products
| Model / number | Product as published |
|---|---|
DYNDV2520 | IV START KIT |
DYNDH1983A | PERIPHERAL LAB BLOOD CULTURE KIT |
ACC010157C | PEDI EMERGENCY TRAY-PURPLE |
ACC010158C | PEDS EMERGENCY TRAY- GREEN |
ACC010159C | PEDI EMERGENCY TRAY-BLUE |
ACC010160C | PEDS EMERGENCY TRAY-YELLOW |
ACC010161C | PEDS EMERGENCY TRAY-WHITE |
ACC010162C | PEDS EMERGENCY TRAY-ORANGE |
ACC010163C | PEDS EMERGENCY TRAY-RED |
ACC010308A | CVHP DRAWER -IV |
ACC010316A | PEDI EMERGENCY TRAY-BLUE |
ACC010318A | PEDS EMERGENCY TRAY- GREEN |
ACC010319A | PEDS EMERGENCY TRAY-ORANGE |
ACC010361 | DRAWER THREE - IV SET UP |
ACC010374A | DRAWER 1 |
ACC010417A | DRAWER 3 LAB DRAW & IV START |
ACC010477B | DRAWER #6 |
ACC010479A | DRAWER #4 |
ACC010679 | ADULT DRAWER 4 |
ACC010690 | DRAWER 2 |
- Lot codes and dates
304 of 304 products
Products covered by this recall # Barcodes Product as published 1 1065316038404500653160384048Lot Number: 2023122690; 2) DYNDV2520, UDI-DI: 10653160384045(each), 00653160384048(case) 2 1065316038404500653160384048Lot Number: 2024020790; 3) DYNDV2520, UDI-DI: 10653160384045(each), 00653160384048(case) 3 1065316038404500653160384048Lot Number: 2024032790; 4) DYNDV2520, UDI-DI: 10653160384045(each), 00653160384048(case) 4 1065316038404500653160384048Lot Number: 2024052390; 5) DYNDV2520, UDI-DI: 10653160384045(each), 00653160384048(case) 5 1065316038404500653160384048Lot Number: 2024071190; 6) DYNDV2520, UDI-DI: 10653160384045(each), 00653160384048(case) 6 1065316038404500653160384048Lot Number: 2024081490; 7) DYNDV2520, UDI-DI: 10653160384045(each), 00653160384048(case) 7 1065316038404500653160384048Lot Number: 2024101090; 8) DYNDV2520, UDI-DI: 10653160384045(each), 00653160384048(case) 8 1065316038892000653160388923Lot Number: 2024111990; 9) DYNDH1983A, UDI-DI: 10653160388920(each), 00653160388923(case) 9 1019532749264940195327492640Lot Number: 2025073190; 10) ACC010157C, UDI-DI: 10195327492649(each), 40195327492640(case) 10 1019532749278640195327492787Lot Number: 23JDB105; 11) ACC010158C, UDI-DI: 10195327492786(each), 40195327492787(case) 11 1019532749277940195327492770Lot Number: 23JDB122; 12) ACC010159C, UDI-DI: 10195327492779(each), 40195327492770(case) 12 1019532749282340195327492824Lot Number: 23JDB078; 13) ACC010160C, UDI-DI: 10195327492823(each), 40195327492824(case) 13 1019532749282340195327492824Lot Number: 23JDA433; 14) ACC010160C, UDI-DI: 10195327492823(each), 40195327492824(case) 14 1019532749281640195327492817Lot Number: 23JDB266; 15) ACC010161C, UDI-DI: 10195327492816(each), 40195327492817(case) 15 1019532749281640195327492817Lot Number: 23JDA587; 16) ACC010161C, UDI-DI: 10195327492816(each), 40195327492817(case) 16 1019532749281640195327492817Lot Number: 23JDB267; 17) ACC010161C, UDI-DI: 10195327492816(each), 40195327492817(case) 17 1019532749279340195327492794Lot Number: 23JDC145; 18) ACC010162C, UDI-DI: 10195327492793(each), 40195327492794(case) 18 1019532749280940195327492800Lot Number: 23JDB106; 19) ACC010163C, UDI-DI: 10195327492809(each), 40195327492800(case) 19 1088994242459740889942424598Lot Number: 23JDB268; 20) ACC010308A, UDI-DI: 10889942424597(each), 40889942424598(case) 20 1088994242459740889942424598Lot Number: 25DDA404; 21) ACC010308A, UDI-DI: 10889942424597(each), 40889942424598(case) - Amount recalled
- 434,595 kits
This recall covers 29 products
The agency filed one notice per product. You are reading one of them; the other 28 are below.
16 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is compromised, patients and users may be exposed to microbial contamination. Potential health consequences may include no injury, localized infection, or, less commonly, more serious infection requiring medical treatment, antimicrobial therapy, procedural intervention, or hospitalization. In rare cases, particularly in critically ill or immunocompromised patients, severe infection could become life-threatening.
This product could cause temporary or reversible health problems — stop using it.
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