FDA Device recall Z-3054-2020
Control, Calibrator Verified, Triage BNP, Model ALR88755
- FDA Device
- Class II
- terminated
- Published 2020-10-07
On 2020-10-07 the FDA classified a Class II recall of Control, Calibrator Verified, Triage BNP, Model ALR88755 by Medline Industries, citing product was shipped with refrigeration (ice) instead of frozen (dry ice).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3054-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-07-28 |
| Published | 2020-10-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medline Industries |
| Distribution | AR, AZ, CO, FL, MD, MI, MS, NC, NM, NY, OK, PA, RI, TX |
Product
Control, Calibrator Verified, Triage BNP, Model ALR88755
Reason
Product was shipped with refrigeration (ice) instead of frozen (dry ice).
Identifiers
| code_info | Lot Number and/or Serial Number: 30718, 407522, 420694, 422646, 430000, 422647N, 422648N, 428255N,428256N, 441421N, 441422N, 441423N |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3054-2020%22
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