Fresh Recalls

FDAClass II · Medical device · Recall Z-2119-2026 · Recalled May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Agency report date: May 13, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Medline Convenience Kits
Company / brand
Medline Industries
Lot / serial / date codes
1) DYNJ50806L, UDI-DI: 10195327344672(each), 40195327344673(case), Lot Number: 23FBK937
Distribution
Worldwide - US Nationwide distribution.
Agency product description and boundaries

Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Medline Convenience Kits

3. Open the official notice or contact

Official recall ID
Z-2119-2026
Brand
Medline Industries
Classification
Class II
Units affected
32 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Northfield, IL, United States
Firm address
3 Lakes Dr, 60093-2753

Identifying details (verbatim from the notice)

Product codes / lots
1) DYNJ50806L, UDI-DI: 10195327344672(each), 40195327344673(case), Lot Number: 23FBK937
Distribution
Worldwide - US Nationwide distribution.
Firm notified the public via
Letter
FDA event ID
98642
Recall initiated
January 7, 2026
FDA classified
May 7, 2026
FDA report date
May 13, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved August 11, 2026 at 6:00 PM UTC.

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