Fresh Recalls

FDAClass II · Medical device · Recall Z-1944-2026 · Recalled May 6, 2026

VACUUM BAG SU LARGE recall — Milestone S.R.L.

Agency report date: May 6, 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
VACUUM BAG SU LARGE
Company / brand
Milestone S.R.L
Lot / serial / date codes
UDI-DI: 08052478981055; Lot Number: 2024-09
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Chile, Israel, UK, Belgium, Spain, France, Greece, Italy, Luxembourg, The Netherlands, Portugal, and Sweden.
Agency product description and boundaries

VACUUM BAG SU LARGE, Non-sterile specimen container, Model/Catalog Number: 68409SS

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: There is a possibility of reagent leakage from the specimen container.

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: VACUUM BAG SU LARGE recall status

3. Open the official notice or contact

Official recall ID
Z-1944-2026
Brand
All Milestone S.R.L recalls
Classification
Class II
Units affected
61600 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Sorisole, Italy
Firm address
Via Fatebenefratelli 1/5, N/A

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI: 08052478981055; Lot Number: 2024-09
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Chile, Israel, UK, Belgium, Spain, France, Greece, Italy, Luxembourg, The Netherlands, Portugal, and Sweden.
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
98632
Recall initiated
March 9, 2026
FDA classified
April 24, 2026
FDA report date
May 6, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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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 August 4, 2026 at 11:00 PM UTC.

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