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
51 of 51 products
| Model / number | Product as published |
|---|---|
DYLAB1081 | BLOOD DRAW KIT |
DYNDB3005D | WHOLE BLOOD PHLEBOTOMY KIT |
DYNDB3005F | QP KIT |
DYNDB3006C | DOUBLE RED CELL PHLEBOTOMY KIT |
DYNDB3007C | PLATELET PHLEBOTOMY KIT |
DYNDB3041D | WHOLE BLOOD KIT |
DYNDB3044D | PHLEBOTOMY |
DYNDB3044F | PHLEBOTOMY |
DYNDB3086D | DONATION - WB |
DYNDB3088B | DONATION - ALYX/TRIMA W/O TOUR |
DYNDB3100 | THERAPEUTIC NFT |
DYNDH1194A | BLOOD CULTURE TRAY ADULT |
DYNDH1444D | ADULT BLOOD CULTURE KIT |
DYNDH1445C | PEDS BLOOD CULTURE KIT |
DYNDH1462B | BLOOD CULTURE KIT |
DYNDH1619A | BLOOD CULTURE ADULT |
DYNDH1620A | BLOOD CULTURE PEDI |
DYNDH1622C | BLOOD CULTURE KIT |
DYNDH1622D | BLOOD CULTURE KIT |
DYNDH1626B | BLOOD CULTURE COLLECTION KIT |
- Lot codes and dates
360 of 360 products
Products covered by this recall # Barcodes Product as published 1 1019532703870040195327038701Lot Number: 25CMC514; 2) DYNDB3005D, UDI-DI: 10195327038700(each), 40195327038701(case) 2 1019532703870040195327038701Lot Number: 24CBG614; 3) DYNDB3005D, UDI-DI: 10195327038700(each), 40195327038701(case) 3 1019532703870040195327038701Lot Number: 24CBT912; 4) DYNDB3005D, UDI-DI: 10195327038700(each), 40195327038701(case) 4 1019532703870040195327038701Lot Number: 23HBH298; 5) DYNDB3005D, UDI-DI: 10195327038700(each), 40195327038701(case) 5 1019532703870040195327038701Lot Number: 23JBN521; 6) DYNDB3005D, UDI-DI: 10195327038700(each), 40195327038701(case) 6 1019845902506840198459025069Lot Number: 23KBT270; 7) DYNDB3005F, UDI-DI: 10198459025068(each), 40198459025069(case) 7 1019845902506840198459025069Lot Number: 25BBD241; 8) DYNDB3005F, UDI-DI: 10198459025068(each), 40198459025069(case) 8 1019845902506840198459025069Lot Number: 25BBP477; 9) DYNDB3005F, UDI-DI: 10198459025068(each), 40198459025069(case) 9 1019845902506840198459025069Lot Number: 25CBI161; 10) DYNDB3005F, UDI-DI: 10198459025068(each), 40198459025069(case) 10 1019845902506840198459025069Lot Number: 24LBM458; 11) DYNDB3005F, UDI-DI: 10198459025068(each), 40198459025069(case) 11 1019845902506840198459025069Lot Number: 24FBL961; 12) DYNDB3005F, UDI-DI: 10198459025068(each), 40198459025069(case) 12 1019845902506840198459025069Lot Number: 24FBS200; 13) DYNDB3005F, UDI-DI: 10198459025068(each), 40198459025069(case) 13 1019532703871740195327038718Lot Number: 24IBO183; 14) DYNDB3006C, UDI-DI: 10195327038717(each), 40195327038718(case) 14 1019532703871740195327038718Lot Number: 24ABB637; 15) DYNDB3006C, UDI-DI: 10195327038717(each), 40195327038718(case) 15 1019532703871740195327038718Lot Number: 24ABY532; 16) DYNDB3006C, UDI-DI: 10195327038717(each), 40195327038718(case) 16 1019532703871740195327038718Lot Number: 24CBH932; 17) DYNDB3006C, UDI-DI: 10195327038717(each), 40195327038718(case) 17 1019532703871740195327038718Lot Number: 23JBN434; 18) DYNDB3006C, UDI-DI: 10195327038717(each), 40195327038718(case) 18 1019532703872440195327038725Lot Number: 23LBH909; 19) DYNDB3007C, UDI-DI: 10195327038724(each), 40195327038725(case) 19 1019532703872440195327038725Lot Number: 24CBL044; 20) DYNDB3007C, UDI-DI: 10195327038724(each), 40195327038725(case) 20 1019532703872440195327038725Lot Number: 23JBC957; 21) DYNDB3007C, UDI-DI: 10195327038724(each), 40195327038725(case) - Amount recalled
- 996692 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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