Fresh Recalls

FDAClass II · Medical device · Recall Z-3209-2026 · Recalled September 23, 2026

Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A recall — Medline Industries, LP

Agency report date: September 23, 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
Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A
Company / brand
Medline Industries
Lot / serial / date codes
UDI-DI 10198459046551 Lot 25FBU754
Distribution
US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
Agency product description and boundaries

Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A

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: Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

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: Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A recall status

3. Open the official notice or contact

Official recall ID
Z-3209-2026
Brand
All Medline Industries recalls
Classification
Class II
Units affected
60
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
UDI-DI 10198459046551 Lot 25FBU754
Distribution
US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
Firm notified the public via
Letter
FDA event ID
99667
Recall initiated
July 31, 2026
FDA classified
September 16, 2026
FDA report date
September 23, 2026

More Medline Industries recalls

Other medical device recalls from around the same time

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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 October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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