Reported Feb 25, 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

70 of 70 products

Products covered by this recall
Model / numberProduct as published
CDS983069GCHP COCHLEAR SUPPLEMENT CDS
CDS983069ICHP COCHLEAR SUPPLEMENT CDS
CDS983782CHEAD & NECK CDS-LF
DYKE1456DBAPTIST FLOYD BRONCHOSCOPY
DYKE1955BRONCHOSCOPY SETUP KIT
DYKMBNDL156KIT ENT HEAD AND NECK GENERIC
DYKMBNDL156AKIT ENT HEAD AND NECK GENERIC
DYKMBNDL156BKIT ENT HEAD AND NECK GENERIC
DYKMBNDL174KIT ENT LARYNGECTOMY
DYKMBNDL174AKIT ENT LARYNGECTOMY
DYKMBNDL174BKIT ENT LARYNGECTOMY
DYKMBNDL196KIT PEDS HEAD AND NECK
DYKMBNDL1AKIT OMF LEFORTE
DYKMBNDL1BKIT OMF LEFORTE
DYKMBNDL1CKIT OMF LEFORTE
DYKMBNDL32KIT ENT ENDOSINUS GENERIC
DYKMBNDL32AKIT ENT ENDOSINUS GENERIC
DYKMBNDL32BKIT ENT ENDOSINUS GENERIC
DYKMBNDL66AKIT GEN SURG THYROIDECTOMY
DYKMBNDL66BKIT GEN SURG THYROIDECTOMY
Lot codes and dates

256 of 256 products

Products covered by this recall
#BarcodesProduct as published
11019348992392640193489923927Lot Number: 21IBD399; 2) CDS983069G, UDI-DI: 10193489923926(each), 40193489923927(case)
21019532707186840195327071869Lot Number: 21HBO921; 3) CDS983069I, UDI-DI: 10195327071868(each), 40195327071869(case)
31019532707186840195327071869Lot Number: 22JBW315; 4) CDS983069I, UDI-DI: 10195327071868(each), 40195327071869(case)
41019532707186840195327071869Lot Number: 22GBE731; 5) CDS983069I, UDI-DI: 10195327071868(each), 40195327071869(case)
51019348959204740193489592048Lot Number: 22FBX804; 6) CDS983782C, UDI-DI: 10193489592047(each), 40193489592048(case)
61019532763993840195327639939Lot Number: 21DKA756; 7) DYKE1456D, UDI-DI: 10195327639938(each), 40195327639939(case)
71019532753983240195327539833Lot Number: 24CBK289; 8) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case)
81019532753983240195327539833Lot Number: 25HLA345; 9) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case)
91019532753983240195327539833Lot Number: 25FLA904; 10) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case)
101019532753983240195327539833Lot Number: 25DLB145; 11) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case)
111019532753983240195327539833Lot Number: 25CLB002; 12) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case)
121019532753983240195327539833Lot Number: 24DLA606; 13) DYKE1955, UDI-DI: 10195327539832(each), 40195327539833(case)
131019348947824240193489478243Lot Number: 24ALA266; 14) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case)
141019348947824240193489478243Lot Number: 21FBS478; 15) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case)
151019348947824240193489478243Lot Number: 21FBO537; 16) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case)
161019348947824240193489478243Lot Number: 21DBJ855; 17) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case)
171019348947824240193489478243Lot Number: 21CBD340; 18) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case)
181019348947824240193489478243Lot Number: 21BBG062; 19) DYKMBNDL156, UDI-DI: 10193489478242(each), 40193489478243(case)
191019348995191240193489951913Lot Number: 21ABK323; 20) DYKMBNDL156A, UDI-DI: 10193489951912(each), 40193489951913(case)
201019348995191240193489951913Lot Number: 22GBH498; 21) DYKMBNDL156A, UDI-DI: 10193489951912(each), 40193489951913(case)
Amount recalled
9051 units

This recall covers 43 products

The agency filed one notice per product. You are reading one of them; the other 42 are below.

30 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:56 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.