Multiphor II Electrophoresis System GE HealthCare Product Number:… — Class II medical device recall Z-2685-2017
Terminated recall by Perkinelmer Life Sciences, Inc., reported 2017-07-12, distributed nationwide. Potential for electric shock in the case of a failure to install the grommets, supplied with the system.
| Recall number | Z-2685-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Perkinelmer Life Sciences, Inc., Boston, MA, United States |
| Recall initiated | 2017-05-15 |
| Classified | 2017-07-04 |
| Reported by FDA | 2017-07-12 |
| Terminated | 2023-03-02 |
| Distributed | Nationwide (US) |
| Quantity | 241 instruments |
| Serial numbers | 1171221, 1171231, 1171232, 1171234, 1181923, 1181925, 1181928, 1187499, 1189475, 1189484, 1195060, 1195074, 1197741, 1197743, 1197752, 1197753, 1200106, 1202993, 1202994, 1251991, 1252000, 1253298, 1253301, 1253307, 1254797 and 63 more |
| Model numbers | 2117-004 |
Product
Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D electrophoresis and electrophoretic transfer Note: The Multiphor II Electrophoresis System (Class I) is the platform used with the hemoglobin electrophoresis gel kit ( Class II) sold by PerkinElmer as the Resolve Hemoglobin Kit (K050709: Product code JJN). The RESOLVE Systems Hemoglobin kit (K050709) is designed to separate whole blood, cord blood or dried blood spot specimen for detection of normal and variant hemoglobins by isoelectric focusing.
Reason for recall
Potential for electric shock in the case of a failure to install the grommets, supplied with 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-2685-2017. 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.