Reported Sep 9, 2026 · Ongoing · Updated Sep 14, 2026

Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number:…

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) ORTHO ASPIRATION KIT
  • Model Number
    • DYKM1636A
    • 2) SHOULD BLOCK KIT
  • Model Number
    • DYKM1881A
    • 3) TRIMA KIT
  • Model NumberDYNDB3077C
Lot codes and dates

22 of 22 products

Products covered by this recall
#BarcodesProduct as published
11088994292585840889942925859Lot Number: 25ABW688; 2) DYKM1636A, UDI-DI: 10889942925858(each), 40889942925859(case)
21019845902517440198459025175Lot Number: 23LBT438; 3) DYKM1881A, UDI-DI: 10198459025174(each), 40198459025175(case)
31019348927380940193489273800Lot Number: 24KBS611; 4) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
41019348927380940193489273800Lot Number: 25BBB106; 5) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
51019348927380940193489273800Lot Number: 24KBJ751; 6) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
61019348927380940193489273800Lot Number: 24LBO630; 7) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
71019348927380940193489273800Lot Number: 24ABB622; 8) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
81019348927380940193489273800Lot Number: 24CBG290; 9) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
91019348927380940193489273800Lot Number: 24CBG291; 10) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
101019348927380940193489273800Lot Number: 24CBT163; 11) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
111019348927380940193489273800Lot Number: 24EBM679; 12) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
121019348927380940193489273800Lot Number: 24FBL963; 13) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
131019348927380940193489273800Lot Number: 24HBV589; 14) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
141019348927380940193489273800Lot Number: 24HBV590; 15) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
151019348927380940193489273800Lot Number: 24HBV591; 16) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
161019348927380940193489273800Lot Number: 24HBV592; 17) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
171019348927380940193489273800Lot Number: 24HBV593; 18) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
181019348927380940193489273800Lot Number: 24JBV697; 19) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
191019348927380940193489273800Lot Number: 24JBV698; 20) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
201019348927380940193489273800Lot Number: 24JBV699; 21) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case)
Amount recalled
18290 kits

This recall covers 29 products

The agency filed one notice per product. You are reading one of them; the other 28 are below.

16 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is compromised, patients and users may be exposed to microbial contamination. Potential health consequences may include no injury, localized infection, or, less commonly, more serious infection requiring medical treatment, antimicrobial therapy, procedural intervention, or hospitalization. In rare cases, particularly in critically ill or immunocompromised patients, severe infection could become life-threatening.

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, 3:39 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.