Reported May 13, 2026 · Ongoing

See RES for complete 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 complete list. Medline Convenience Kits

8 of 8 products

Products covered by this recall
Model / numberProduct as published
ACC010499PLASTIC BIN W/MISC KITS
CDS984853JBREAST-HERNIA-PORT CDS-LF
DYKMBNDL117CKIT UROLOGY URETHROPLASTY
DYKMBNDL158KIT PLASTIC INSERT TISSUE EXPA
DYKMBNDL170KIT PLASTIC ABDOMINOPLASTY
DYKMBNDL170AKIT PLASTIC ABDOMINOPLASTY
DYKMBNDL170BKIT PLASTIC ABDOMINOPLASTY
DYKMBNDL182KIT PLASTIC ABDOMINOPLASTY
Lot codes and dates

277 of 277 products

Products covered by this recall
#BarcodesProduct as published
11019348984570940193489845700Lot Number: 21DDA661; 2) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
21019348984570940193489845700Lot Number: 21FDA888; 3) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
31019348984570940193489845700Lot Number: 21GDB740; 4) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
41019348984570940193489845700Lot Number: 21HDB434; 5) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
51019348984570940193489845700Lot Number: 21JDB530; 6) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
61019348984570940193489845700Lot Number: 23HDB786; 7) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
71019348984570940193489845700Lot Number: 23IDB182; 8) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
81019348984570940193489845700Lot Number: 23LDC086; 9) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
91019348984570940193489845700Lot Number: 24IDA403; 10) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
101019348984570940193489845700Lot Number: 24JDA650; 11) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
111019348984570940193489845700Lot Number: 25ADB705; 12) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
121019348984570940193489845700Lot Number: 25BDA228; 13) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
131019348984570940193489845700Lot Number: 25BDB702; 14) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
141019348984570940193489845700Lot Number: 25FDA013; 15) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case)
151019532769418040195327694181Lot Number: 25GDB671; 16) CDS984853J, UDI-DI: 10195327694180(each), 40195327694181(case)
161019532769418040195327694181Lot Number: 24DDC169; 17) CDS984853J, UDI-DI: 10195327694180(each), 40195327694181(case)
171019532737110440195327371105Lot Number: 24EDA131; 18) DYKMBNDL117C, UDI-DI: 10195327371104(each), 40195327371105(case)
181019348947826640193489478267Lot Number: 23DLA834; 19) DYKMBNDL158, UDI-DI: 10193489478266(each), 40193489478267(case)
191019348947826640193489478267Lot Number: 21ABI978; 20) DYKMBNDL158, UDI-DI: 10193489478266(each), 40193489478267(case)
201019348947745040193489477451Lot Number: 21CBE548; 21) DYKMBNDL170, UDI-DI: 10193489477450(each), 40193489477451(case)
Amount recalled
5497 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, 5:39 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.