Fresh Recalls

FDAClass II · Medical device · Recall Z-1888-2026 · Recalled April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ART recall — Medline Industries, LP

Agency report date: April 29, 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 containing select SKUs of 10mL Polycarbonate Colored Syringes ART
Company / brand
Medline Industries
Lot / serial / date codes
DYNJ45173D UDI-DI 10889942485222 (EA) 40889942485223 (CS) LOT 24BBB811
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.
Agency product description and boundaries

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ARTHROSCOPY PACK DYNJ45173D

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: Unapproved design changes to the products outside of the 510(k) clearance.

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 containing select SKUs of 10mL Polycarbonate Colored Syringes ART

3. Open the official notice or contact

Official recall ID
Z-1888-2026
Brand
Medline Industries
Classification
Class II
Units affected
270,311 total
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

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

Identifying details (verbatim from the notice)

Product codes / lots
DYNJ45173D UDI-DI 10889942485222 (EA) 40889942485223 (CS) LOT 24BBB811
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.
Firm notified the public via
Letter
FDA event ID
98601
Recall initiated
February 27, 2026
FDA classified
April 17, 2026
FDA report date
April 29, 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 July 28, 2026 at 11:00 PM UTC.

Report a data error on this page