---
title: "BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL — FDA record Z-0807-2022 | Is It on Recall"
description: "Due to current concerns related to COVID-19 vaccine interference with the RPR portion of the BioPlex 2200 Syphilis Total & RPR panel, as well as intermittent ma"
url: https://isitonrecall.com/recall/fda-device-z-0807-2022-bioplex-2200-ref-12000651-syphilis-total-rpr-calibrator-set-cal/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL — FDA record Z-0807-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 8, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL
- **Reason**: Due to current concerns related to COVID-19 vaccine interference with the RPR portion of the BioPlex 2200 Syphilis Total & RPR panel, as well as intermittent manufacturing challenges to produce RPR reagents that consistently meet stability specifications
- **Classification**: Class II
- **Recalling firm**: Bio-Rad Laboratories, Inc.
- **Quantity**: 724 Calibrator sets (U.S.)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0807-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0807-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Catalog Number: 12000651 UDI GTIN Code: 03610520652770 Lot Numbers: 53262 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution U.S. Nationwide distribution in the states of AK, AL, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WV. The countries of France, Germany, Italy, Spain, Saudi Arabia, and United Arab Emirates.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Mar 23, 2022
- **Recall initiation date**: Feb 8, 2022
- **Center classification date**: Mar 16, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0807-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Bio-Rad Laboratories, Inc. records](https://isitonrecall.com/brand/bio-rad-laboratories-inc/)
