FDA Device recall Z-3032-2026
healthmark ProChek-W Protein Test for Robotic Arms
- FDA Device
- Class II
- ongoing
- Published 2026-09-02
On 2026-09-02 the FDA classified a Class II recall of healthmark ProChek-W Protein Test for Robotic Arms by Healthmark Industries, citing test manufactured with an expired ingredient which may present as either a false negative or positive.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3032-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-29 |
| Published | 2026-09-02 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Healthmark Industries |
| Distribution | US |
Product
healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001
Reason
Test manufactured with an expired ingredient which may present as either a false negative or positive.
Identifiers
| code_info | Serial/Lot Numbers: 200035, 200036, 200037, 200038, 200039, 200040, 30028. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3032-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.