Perkinelmer
Complete recall history across all FDA and CPSC categories — 20 total recalls
Perkinelmer appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (20)
FDA medical device enforcement actions by Perkinelmer
| Date | Product | Reason | Class |
|---|---|---|---|
| Dec 8, 2015 | Perkin Elmer ClWIZARD2 5-detector, 550 samples Product Code: 2470-0050, 3470... | The content of the second #023 barcode ID label in the Barcode ID Label Binde... | Class II |
| Dec 8, 2015 | Perkin Elmer WIZARD2 2-detector, 550 samples Product Code: 2470-0020 The Wiz... | The content of the second #023 barcode ID label in the Barcode ID Label Binde... | Class II |
| Dec 8, 2015 | Perkin Elmer WIZARD2 10-detector, 1000 samples. Product Code: 2470-0200, 347... | The content of the second #023 barcode ID label in the Barcode ID Label Binde... | Class II |
| Dec 8, 2015 | Perkin Elmer WIZARD2 5-detector, 1000 samples Product Code: 2470-0150, 3470-... | The content of the second #023 barcode ID label in the Barcode ID Label Binde... | Class II |
| Dec 8, 2015 | Perkin Elmer WIZARD2 1-detector,3", 1000 samples. Product Code: 2480-0010 T... | The content of the second #023 barcode ID label in the Barcode ID Label Binde... | Class II |
| Dec 8, 2015 | Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The Wiz... | The content of the second #023 barcode ID label in the Barcode ID Label Binde... | Class II |
| Dec 8, 2015 | Perkin Elmer WIZARD2 10-detector, 550 samples Product Code: 2470-0100, 3470-0... | The content of the second #023 barcode ID label in the Barcode ID Label Binde... | Class II |
| Jun 3, 2015 | WIZARD2 5-detector, 550 samples Product Code: 2470-0050, 3470-0050 The Wi... | Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results | Class II |
| Jun 3, 2015 | WIZARD2 2-detector, 550 samples Product Code: 2470-0020 The Wizard¿" gamm... | Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results | Class II |
| Jun 3, 2015 | Perkin Elmer WIZARD2 10-detector, 1000 samples Product Code: 2470-0200, 3470... | Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results | Class II |
| Jun 3, 2015 | Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The ... | Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results | Class II |
| Jun 3, 2015 | Perkin Elmer WIZARD2 5-detector, 1 000 samples Product Code: 2470-0150, 3470... | Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results | Class II |
| Jun 3, 2015 | Perkin Elmer WIZARD2 1-detector,3", 1000 samples Product Code: 2480-0010 ... | Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results | Class II |
| Jun 3, 2015 | Perkin Elmer WIZARD2 10-detector, 550 samples Product Code: 2470-0100, 3470-... | Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results | Class II |
| Nov 26, 2012 | NEOBASE NON-DERIVATIZED MSMS KIT Product Number: ... | Truncated V-Bottomed Microplate Wells used in assays contain defective wells. | Class II |
| Nov 26, 2012 | Microplate, truncated V-bottomed lots included in the above listed products ... | Truncated V-Bottomed Microplate Wells used in assays contain defective wells. | Class II |
| Nov 26, 2012 | NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT Produc... | Truncated V-Bottomed Microplate Wells used in assays contain defective wells. | Class II |
| Nov 26, 2012 | DBS MICROPLATE, TRUNCATED V-BOTTOMED Product Number: 3033-0010 | Truncated V-Bottomed Microplate Wells used in assays contain defective wells. | Class II |
| Nov 26, 2012 | NEONATAL TOTAL GALACTOSE KIT Product Numb... | Truncated V-Bottomed Microplate Wells used in assays contain defective wells. | Class II |
| Jun 27, 2012 | Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Pr... | Contamination from GSP Shaker unit results in decreased signal activity of as... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.
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