Fresh Recalls

FDAClass II · Medical device · Recall Z-2275-2026 · Recalled June 10, 2026

PhaseOne Antimicrobial Solution recall — Oculus Technologies of Mexico, S.A. de C.V.

Agency report date: June 10, 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
PhaseOne Antimicrobial Solution
Company / brand
Oculus Technologies of Mexico
Lot / serial / date codes
UDI:00860009268616 Lot: 25G263
Distribution
US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.
Agency product description and boundaries

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

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: The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.

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: PhaseOne Antimicrobial Solution recall status

3. Open the official notice or contact

Official recall ID
Z-2275-2026
Brand
All Oculus Technologies of Mexico recalls
Classification
Class II
Units affected
5904 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Zapopan, Mexico
Firm address
Calle Industria Vidriera 81, Industrial Zapopan Norte, N/A

Identifying details (verbatim from the notice)

Product codes / lots
UDI:00860009268616 Lot: 25G263
Distribution
US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.
FDA event ID
98959
Recall initiated
April 27, 2026
FDA classified
June 1, 2026
FDA report date
June 10, 2026

Other medical device recalls from around the same time

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 October 22, 2026 at 6:00 PM UTC. Record retrieved September 8, 2026 at 6:00 PM UTC.

Report a data error on this page