PR4100 Microplate Reader US — Class II medical device recall Z-2541-2018
Terminated recall by Bio-Rad Laboratories Inc, reported 2018-08-01, distributed nationwide. The connector of the power supply was capable of fitting other components provided with the system. However, t
| Recall number | Z-2541-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bio-Rad Laboratories Inc, Redmond, WA, United States |
| Recall initiated | 2018-04-02 |
| Classified | 2018-07-25 |
| Reported by FDA | 2018-08-01 |
| Distributed | Nationwide (US) |
| Quantity | 153 |
| UPC / GTIN / UDI-DI | 00847865014151 |
| Serial numbers | 1112001938, 1112001941, 1112004075, 1112004079, 1112004083, 1112004084, 1112004086, 1112004088, 1112004093, 1201003822, 1201003826, 1201003827, 1207001007, 1207001015, 1207001017, 1207001018, 1208001583, 1208001584, 1208001586, 1208001590, 1208005236, 1208005244, 1208005245, 1211000978, 1211000983 and 128 more |
| Model numbers | 45591587 |
Product
PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well absorbance reader for the measurement of light absorbance (optical density-OD) of liquid media. The instrument is intended to be used primarily for the in vitro diagnostic analysis of samples from the human body to obtain information oh physiological and pathological states.
Reason for recall
The connector of the power supply was capable of fitting other components provided with the system. However, the voltage output of the reader power supply is incompatible with the other component and, if incorrectly connected, could result in irreparable damage to the system.
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-2541-2018. 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.