WIZARD2 5-detector — Class II medical device recall Z-2126-2015
Terminated recall by Perkinelmer, reported 2015-07-29, distributed nationwide. Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
| Recall number | Z-2126-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Perkinelmer, Waltham, MA, United States |
| Recall initiated | 2015-06-03 |
| Classified | 2015-07-20 |
| Reported by FDA | 2015-07-29 |
| Terminated | 2017-08-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BE, BR, CA, CH, CL, CN, CR, CZ, DE, DK, ES, FI, FR, GB, GR, HK, HR, HU, IE, IL, IN, IT, JP, KR, KW, LU, MX, NL, NO, PH, PL, SE, SG, TH, TR, TW, ZA |
| Quantity | 53 units |
| Reason classes | labeling |
| Serial numbers | DG03130211, DG04130287, DG05130344, DG06129306, DG08129516, DG08129541, DG08129542, DG08129582, DG08129593, DG10129714, DG10129720, DG11095720, DG12118684, DG12129915, DG12129916, DG12129917, DG12129918, SG24700050, SGWZ01150227, SGWZ02150229, SGWZ02150230, SGWZ03150232, SGWZ04140102, SGWZ06140105, SGWZ10150251 and 28 more |
Product
WIZARD2 5-detector, 550 samples Product Code: 2470-0050, 3470-0050 The Wizard¿" gamma counter is intended to detect and count gamma radiation emitted by clinical samples.
Reason for recall
Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
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-2126-2015. 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.