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

40 of 40 products

Products covered by this recall
Model / numberProduct as published
DYKMBNDL104KIT OPHTHALMIC RUPTURE GLOBE
DYKMBNDL104AKIT OPHTHALMIC RUPTURE GLOBE
DYKMBNDL159KIT OPHTHALMOLOGY CORNEAL TRAN
DYKMBNDL180KIT OPHTHALMOLOGY CATARACT
DYKMBNDL42KIT OPHTHALMOLOGY EYE MUSCLE
DYKMBNDL43BKIT SURG ONC PORT INSERTION
DYKMBNDL84BKIT SURG ONC EXCISION BREAST
DYKMBNDL98KIT OPTHAMOLOGY BASIC
DYKMBNDL98AKIT OPTHAMOLOGY BASIC
DYKMBNDL98BKIT OPTHAMOLOGY BASIC
DYNJ17004LCAROMONT EYE TRAY-LF
DYNJ17219CMINOR EYE PACK
DYNJ38791MPEDS EYE/MUSCLE PACK
DYNJ41207CEYE PACK
DYNJ42043IOPHTHALMIC PACK
DYNJ44852JBREAST RECONSTRUCTION-HOULE
DYNJ45585CCUSTOM EYE PACK HA-LF
DYNJ47859BEYE PLASTIC PACK
DYNJ47859CEYE PLASTIC PACK
DYNJ53019ACATARACT PACK
Lot codes and dates

137 of 137 products

Products covered by this recall
#BarcodesProduct as published
11019348947894540193489478946Lot Number: 21ABV400; 2) DYKMBNDL104, UDI-DI: 10193489478945(each), 40193489478946(case)
21019348947894540193489478946Lot Number: 21FBP706; 3) DYKMBNDL104, UDI-DI: 10193489478945(each), 40193489478946(case)
31019348947894540193489478946Lot Number: 21IBV636; 4) DYKMBNDL104, UDI-DI: 10193489478945(each), 40193489478946(case)
41019532724062240195327240623Lot Number: 22GBP895; 5) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case)
51019532724062240195327240623Lot Number: 22HBX475; 6) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case)
61019532724062240195327240623Lot Number: 22JBS899; 7) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case)
71019532724062240195327240623Lot Number: 22JBS907; 8) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case)
81019532724062240195327240623Lot Number: 22KBO773; 9) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case)
91019532724062240195327240623Lot Number: 23HBV380; 10) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case)
101019532724062240195327240623Lot Number: 24EBU650; 11) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case)
111019348947827340193489478274Lot Number: 25HBK503; 12) DYKMBNDL159, UDI-DI: 10193489478273(each), 40193489478274(case)
121019348947846440193489478465Lot Number: 21ABQ655; 13) DYKMBNDL180, UDI-DI: 10193489478464(each), 40193489478465(case)
131019348947846440193489478465Lot Number: 21ABT655; 14) DYKMBNDL180, UDI-DI: 10193489478464(each), 40193489478465(case)
141019348947846440193489478465Lot Number: 21BBM375; 15) DYKMBNDL180, UDI-DI: 10193489478464(each), 40193489478465(case)
151019348947888440193489478885Lot Number: 21FBP773; 16) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case)
161019348947888440193489478885Lot Number: 21ABR620; 17) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case)
171019348947888440193489478885Lot Number: 21BBK655; 18) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case)
181019348947888440193489478885Lot Number: 21FLA394; 19) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case)
191019348947888440193489478885Lot Number: 21HLA179; 20) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case)
201019348947888440193489478885Lot Number: 21ILA655; 21) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case)
Amount recalled
7760 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 5:34 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.