# FDA recall Z-2169-2026

> **Quidel Corporation** · Class II · device recall initiated 2026-04-06.

## Product

QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.

## Reason for recall

Product has the potential for false positive results

## Distribution

US Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA.

## Key facts

- **Recall number:** Z-2169-2026
- **Recalling firm:** Quidel Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-06
- **Report date:** 2026-05-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2169-2026

## Citation

> MORVS. FDA recall Z-2169-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-2169-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*