Reported May 13, 2026 · Ongoing

Medline Convenience Kits: 1) DYNDA3003, Model Number: DENTAL PACK; 2) DYNJ87157, Model Number: GULLO SURGICAL PACK

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) DYNDA3003
  • Model NumberDENTAL PACK; 2) DYNJ87157
  • Model NumberGULLO SURGICAL PACK
Lot codes and dates

20 of 20 products

Products covered by this recall
#BarcodesProduct as published
11019532725748440195327257485Lot Number: 22JBH446; 2) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
21019532725748440195327257485Lot Number: 23ABA768; 3) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
31019532725748440195327257485Lot Number: 23BBS986; 4) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
41019532725748440195327257485Lot Number: 23CBN951; 5) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
51019532725748440195327257485Lot Number: 23CBT510; 6) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
61019532725748440195327257485Lot Number: 23CBV199; 7) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
71019532725748440195327257485Lot Number: 23GBA134; 8) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
81019532725748440195327257485Lot Number: 23JBH393; 9) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
91019532725748440195327257485Lot Number: 24BBH600; 10) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
101019532725748440195327257485Lot Number: 24CMF059; 11) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
111019532725748440195327257485Lot Number: 24CMF059A; 12) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
121019532725748440195327257485Lot Number: 24EMC989; 13) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
131019532725748440195327257485Lot Number: 24HME376; 14) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
141019532725748440195327257485Lot Number: 24JMG165; 15) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
151019532725748440195327257485Lot Number: 24KMH629; 16) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
161019532725748440195327257485Lot Number: 25AMD692; 17) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
171019532725748440195327257485Lot Number: 25EMB013; 18) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
181019532725748440195327257485Lot Number: 25FMI462; 19) DYNDA3003, UDI-DI: 10195327257484(each), 40195327257485(case)
191019845901448240198459014483Lot Number: 25HMH340; 20) DYNJ87157, UDI-DI: 10198459014482(each), 40198459014483(case)
20Lot Number: 24ILA361
Amount recalled
3508 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, 7:35 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.