FDA Device recall Z-2541-2018
PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well absorbance reader for the mea…
- FDA Device
- Class II
- terminated
- Published 2018-08-01
On 2018-08-01 the FDA classified a Class II recall of PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well absorbance reader for the mea… by Bio Rad Laboratories, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2541-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-04-02 |
| Published | 2018-08-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Bio Rad Laboratories |
| Distribution | US |
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
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.
Identifiers
| code_info | UDI: 00847865014151 Serial Numbers: 140600072, 160900991, 161001953, 1112001938, 1112001941 , 1112004075…UDI: 00847865014151 Serial Numbers: 140600072, 160900991, 161001953, 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 , 1211006938 , 1301003205 , 1301003212 , 1303000299 , 1303000300 , 1303000302 , 1303000305 , 1303007688 , 1306003195 , 1307006044 , 1307006045 , 1307006054 , 1307006055 , 1308000967 , 1308000968 , 1308000969 , 1308000971 , 1308000973 , 1308003338 , 1308003341 , 1308003345 , 1308003346 , 1308006670 , 1311008542 , 1311008544 , 1311008546 , 1311008555 , 1311008557 , 1311008562 , 1311008564 , 1311008565 , 1401002580 , 1401002583 , 1401002587 , 1401007785 , 1401007786 , 140100 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2541-2018%22
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