Fresh Recalls

FDAClass II · Medical device · Recall Z-3032-2026 · Recalled September 2, 2026

healthmark ProChek-W Protein Test for Robotic Arms recall — Healthmark Industries Co., Inc.

Agency report date: September 2, 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
healthmark ProChek-W Protein Test for Robotic Arms
Company / brand
Healthmark Industries Co
Lot / serial / date codes
Serial/Lot Numbers: 200035, 200036, 200037, 200038, 200039, 200040, 30028.
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, France, Hong Kong, South Korea.
Agency product description and boundaries

healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001

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: Test manufactured with an expired ingredient which may present as either a false negative or positive.

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: healthmark ProChek-W Protein Test for Robotic Arms recall status

3. Open the official notice or contact

Official recall ID
Z-3032-2026
Brand
All Healthmark Industries Co recalls
Classification
Class II
Units affected
53 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Fraser, MI, United States
Firm address
18600 Malyn Blvd, N/A, 48026-3496

Identifying details (verbatim from the notice)

Product codes / lots
Serial/Lot Numbers: 200035, 200036, 200037, 200038, 200039, 200040, 30028.
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, France, Hong Kong, South Korea.
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99537
Recall initiated
July 29, 2026
FDA classified
August 26, 2026
FDA report date
September 2, 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 October 22, 2026 at 6:00 PM UTC.

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