Reported May 13, 2026 · Ongoing
See RES for full list. 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?
See RES for full list. Medline Convenience Kits
8 of 8 products
| Model / number | Product as published |
|---|---|
CDS983069G | CHP COCHLEAR SUPPLEMENT CDS |
CDS983069I | CHP COCHLEAR SUPPLEMENT CDS |
CDS983782C | HEAD & NECK CDS-LF |
DYKE1456D | BAPTIST FLOYD BRONCHOSCOPY |
DYKE1955 | BRONCHOSCOPY SETUP KIT |
DYKMBNDL156 | KIT ENT HEAD AND NECK GENERIC |
DYKMBNDL156A | KIT ENT HEAD AND NECK GENERIC |
DYKMBNDL156B | KIT ENT HEAD AND NECK GENERIC |
- Lot codes and dates
307 of 307 products
Products covered by this recall # Barcodes Product as published 1 1019348992392640193489923927Lot Number: 21HBO921; 2) CDS983069G, UDI-DI: 10193489923926(each), 40193489923927(case) 2 1019532707186840195327071869Lot Number: 21IBD399; 3) CDS983069I, UDI-DI: 10195327071868(each), 40195327071869(case) 3 1019532707186840195327071869Lot Number: 22FBX804; 4) CDS983069I, UDI-DI: 10195327071868(each), 40195327071869(case) 4 1019532707186840195327071869Lot Number: 22GBE731; 5) CDS983069I, UDI-DI: 10195327071868(each), 40195327071869(case) 5 1019348959204740193489592048Lot Number: 22JBW315; 6) CDS983782C, UDI-DI: 10193489592047(each), 40193489592048(case) 6 1019532763993840195327639939Lot Number: 21DKA756; 7) DYKE1456D, UDI-DI: 10195327639938(each), 40195327639939(case) 7 1019532753983240195327539833Lot Number: 24CBK289; 8) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case) 8 1019532753983240195327539833Lot Number: 24ALA266; 9) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case) 9 1019532753983240195327539833Lot Number: 24DLA606; 10) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case) 10 1019532753983240195327539833Lot Number: 25CLB002; 11) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case) 11 1019532753983240195327539833Lot Number: 25DLB145; 12) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case) 12 1019532753983240195327539833Lot Number: 25FLA904; 13) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case) 13 1019348947824240193489478243Lot Number: 25HLA345; 14) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case) 14 1019348947824240193489478243Lot Number: 21ABK323; 15) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case) 15 1019348947824240193489478243Lot Number: 21BBG062; 16) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case) 16 1019348947824240193489478243Lot Number: 21CBD340; 17) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case) 17 1019348947824240193489478243Lot Number: 21DBJ855; 18) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case) 18 1019348947824240193489478243Lot Number: 21FBO537; 19) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case) 19 1019348995191240193489951913Lot Number: 21FBS478; 20) DYKMBNDL156A, UDI-DI: 10193489951912(each), 40193489951913(case) 20 1019348995191240193489951913Lot Number: 21GBE737; 21) DYKMBNDL156A, UDI-DI: 10193489951912(each), 40193489951913(case) - Amount recalled
- 11575 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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