Reported Feb 25, 2026 · Ongoing

Medline Convenience Kits: 1) PPE KIT, Model Number: DYK1011945P

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 Kits1) PPE KIT
  • Model NumberDYK1011945P
Lot codes and dates

29 of 29 products

Products covered by this recall
#BarcodesProduct as published
11088438938997340884389389974Lot Number: 25IFA006; 2) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
21088438938997340884389389974Lot Number: 24GFA027; 3) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
31088438938997340884389389974Lot Number: 24FFA115; 4) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
41088438938997340884389389974Lot Number: 24BFA115; 5) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
51088438938997340884389389974Lot Number: 23LFA050; 6) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
61088438938997340884389389974Lot Number: 23GFA079; 7) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
71088438938997340884389389974Lot Number: 23EFA070; 8) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
81088438938997340884389389974Lot Number: 23EFA007; 9) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
91088438938997340884389389974Lot Number: 23DFA024; 10) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
101088438938997340884389389974Lot Number: 23CFA070; 11) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
111088438938997340884389389974Lot Number: 23BFA124; 12) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
121088438938997340884389389974Lot Number: 23BFA006; 13) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
131088438938997340884389389974Lot Number: 23AFA090; 14) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
141088438938997340884389389974Lot Number: 23AFA049; 15) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
151088438938997340884389389974Lot Number: 22LFA068; 16) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
161088438938997340884389389974Lot Number: 22JFA111; 17) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
171088438938997340884389389974Lot Number: 22IFA036; 18) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
181088438938997340884389389974Lot Number: 22DFA081; 19) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
191088438938997340884389389974Lot Number: 22CFA086; 20) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
201088438938997340884389389974Lot Number: 22BFA066; 21) DYK1011945P, UDI-DI: 10884389389973(each), 40884389389974(case)
Amount recalled
7575 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, 7:36 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.