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

38 of 38 products

Products covered by this recall
Model / numberProduct as published
CDS982407NBAP NORTH ROBOTIC SURGERY CDS
CDS982407NBAP NORTH ROBOTIC SURGERY CDS
CDS985431JTOT/ GYN LITHOTOMY CDS
CDS985431KTOT/ GYN LITHOTOMY CDS
CDS985431LTOT/ GYN LITHOTOMY CDS
CDS985431NTOT/ GYN LITHOTOMY CDS
CDS985431OTOT/ GYN LITHOTOMY CDS
DYKMBNDL109AKIT ROBOTICS GYN
DYKMBNDL116AKIT ROBOTICS UROLOGY PROSTATE
DYKMBNDL116GKIT ROBOTICS UROLOGY PROSTATE
DYNJ04135BROBOTIC PACK
DYNJ04382JMINOR LITHOTOMY PACK
DYNJ0665843CNBMC D & C PACK-LF
DYNJ22567GD&C PACK-LF
DYNJ22567ID&C PACK-LF
DYNJ22567JD&C PACK-LF
DYNJ22567KD&C PACK-LF
DYNJ38805BD&C HYSTEROSCOPY PACK
DYNJ41272BD AND C
DYNJ41272CD AND C
Lot codes and dates

203 of 203 products

Products covered by this recall
#BarcodesProduct as published
11019348968300440193489683005Lot Number: 21CBD150; 2) CDS982407N, UDI-DI: 10193489683004(each), 40193489683005(case)
21019532733611040195327336111Lot Number: 21DBO201; 3) CDS985431J, UDI-DI: 10195327336110(each), 40195327336111(case)
31019532733611040195327336111Lot Number: 23BBG608; 4) CDS985431J, UDI-DI: 10195327336110(each), 40195327336111(case)
41019532733611040195327336111Lot Number: 23DBM469; 5) CDS985431J, UDI-DI: 10195327336110(each), 40195327336111(case)
51019532745129540195327451296Lot Number: 23FBA948; 6) CDS985431K, UDI-DI: 10195327451295(each), 40195327451296(case)
61019532745129540195327451296Lot Number: 23GBL932; 7) CDS985431K, UDI-DI: 10195327451295(each), 40195327451296(case)
71019532745129540195327451296Lot Number: 23GBM332; 8) CDS985431K, UDI-DI: 10195327451295(each), 40195327451296(case)
81019532745129540195327451296Lot Number: 23IBQ647; 9) CDS985431K, UDI-DI: 10195327451295(each), 40195327451296(case)
91019532752727340195327527274Lot Number: 23JBF512; 10) CDS985431L, UDI-DI: 10195327527273(each), 40195327527274(case)
101019532752727340195327527274Lot Number: 24ABA205; 11) CDS985431L, UDI-DI: 10195327527273(each), 40195327527274(case)
111019532752727340195327527274Lot Number: 24ABV349; 12) CDS985431L, UDI-DI: 10195327527273(each), 40195327527274(case)
121019532752727340195327527274Lot Number: 24ABW239; 13) CDS985431L, UDI-DI: 10195327527273(each), 40195327527274(case)
131019532752727340195327527274Lot Number: 24CBR704; 14) CDS985431L, UDI-DI: 10195327527273(each), 40195327527274(case)
141019845908159040198459081591Lot Number: 24EBP485; 15) CDS985431N, UDI-DI: 10198459081590(each), 40198459081591(case)
151019845919500640198459195007Lot Number: 24JBG321; 16) CDS985431O, UDI-DI: 10198459195006(each), 40198459195007(case)
161019845919500640198459195007Lot Number: 24LBH099; 17) CDS985431O, UDI-DI: 10198459195006(each), 40198459195007(case)
171019845919500640198459195007Lot Number: 25ABT899; 18) CDS985431O, UDI-DI: 10198459195006(each), 40198459195007(case)
181019845919500640198459195007Lot Number: 25CBE670; 19) CDS985431O, UDI-DI: 10198459195006(each), 40198459195007(case)
191019845919500640198459195007Lot Number: 25EBE265; 20) CDS985431O, UDI-DI: 10198459195006(each), 40198459195007(case)
201019845919500640198459195007Lot Number: 25GBB847; 21) CDS985431O, UDI-DI: 10198459195006(each), 40198459195007(case)
Amount recalled
13376 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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:47 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.