Control — Class II medical device recall Z-3054-2020
Terminated recall by Medline Industries Inc, reported 2020-10-07, distributed in AR, AZ, CO, FL, MD, MI, MS, NC…. Product was shipped with refrigeration (ice) instead of frozen (dry ice).
| Recall number | Z-3054-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2020-07-28 |
| Classified | 2020-09-30 |
| Reported by FDA | 2020-10-07 |
| Terminated | 2023-02-13 |
| Distributed | AR, AZ, CO, FL, MD, MI, MS, NC, NM, NY, OK, PA, RI, TX |
| Quantity | 118 units |
| Serial numbers | 30718, 407522, 420694, 422646, 422647N, 422648N, 428255N, 428256N, 430000, 441421N, 441422N, 441423N |
| Model numbers | ALR88755 |
Product
Control, Calibrator Verified, Triage BNP, Model ALR88755
Reason for recall
Product was shipped with refrigeration (ice) instead of frozen (dry ice).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3054-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.