Reported May 13, 2026 · Ongoing
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
52 of 52 products
| Model / number | Product as published |
|---|---|
CDS860018G | NEURO SHUNT- CODMAN |
CDS860018I | NEURO SHUNT- CODMAN |
DYKMBNDL138 | KIT NEUR FUS LUM POST CRANDALL |
DYKMBNDL142 | KIT NEURO FUS LUM POST SANSUR |
DYKMBNDL142B | KIT NEURO FUS LUM POST SANSUR |
DYKMBNDL145 | KIT NEURO DECOMPRESSIVE CRANIO |
DYKMBNDL145B | KIT NEURO DECOMPRESSIVE CRANIO |
DYKMBNDL5 | KIT NEURO TRANSPHENOIDAL |
DYKMBNDL5B | KIT NEURO TRANSPHENOIDAL |
DYNJ0305809O | NEURO PACK-LF |
DYNJ0305809P | NEURO PACK-LF |
DYNJ0408776Y | NEURO PACK-LF |
DYNJ04596K | NEURO PACK-LF |
DYNJ0781823K | NEURO/LAMINECTOMY BASIN PK-LF |
DYNJ35243L | BASIC NEURO PACK SMMC-LF |
DYNJ49098I | NEURO PACK |
DYNJ53089B | NEURO PACK |
DYNJ53799 | NEURO LAMINECTOMY-LF |
DYNJ58704A | NEURO MINOR PACK-UNIV |
DYNJ60100C | NEURO PACK - IFCAP 230316 |
- Lot codes and dates
324 of 324 products
Products covered by this recall # Barcodes Product as published 1 1088994245964340889942459644Lot Number: 21CBA213; 2) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 2 1088994245964340889942459644Lot Number: 21DBD719; 3) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 3 1088994245964340889942459644Lot Number: 21GMA403; 4) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 4 1088994245964340889942459644Lot Number: 21GME436; 5) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 5 1088994245964340889942459644Lot Number: 21GMF497; 6) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 6 1088994245964340889942459644Lot Number: 21JMH357; 7) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 7 1088994245964340889942459644Lot Number: 21KMD971; 8) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 8 1088994245964340889942459644Lot Number: 21LMG598; 9) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 9 1088994245964340889942459644Lot Number: 22DMD555; 10) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 10 1088994245964340889942459644Lot Number: 22HMC764; 11) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 11 1088994245964340889942459644Lot Number: 22KMF991; 12) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 12 1088994245964340889942459644Lot Number: 23AMJ086; 13) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 13 1088994245964340889942459644Lot Number: 23CMD444; 14) CDS860018G, UDI-DI: 10889942459643(each), 40889942459644(case) 14 1019532738177640195327381777Lot Number: 23CMH970; 15) CDS860018I, UDI-DI: 10195327381776(each), 40195327381777(case) 15 1019532738177640195327381777Lot Number: 23EME270; 16) CDS860018I, UDI-DI: 10195327381776(each), 40195327381777(case) 16 1019532738177640195327381777Lot Number: 23GMC110; 17) CDS860018I, UDI-DI: 10195327381776(each), 40195327381777(case) 17 1019532738177640195327381777Lot Number: 23IME897; 18) CDS860018I, UDI-DI: 10195327381776(each), 40195327381777(case) 18 1019532738177640195327381777Lot Number: 23JMA572; 19) CDS860018I, UDI-DI: 10195327381776(each), 40195327381777(case) 19 1019532738177640195327381777Lot Number: 23JMI786; 20) CDS860018I, UDI-DI: 10195327381776(each), 40195327381777(case) 20 1019532738177640195327381777Lot Number: 23KMB758; 21) CDS860018I, UDI-DI: 10195327381776(each), 40195327381777(case) - Amount recalled
- 10184 units
This recall covers 42 products
The agency filed one notice per product. You are reading one of them; the other 41 are below.
29 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
This product could cause temporary or reversible health problems — stop using it.
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