# FDA recall Z-2444-2025

> **Orascoptic Surgical Acuity** · Class II · device recall initiated 2025-07-03.

## Product

Orascoptic Superior Visualization  Dragonfly Nose Pad Accessory Kit ( nose pad and screw)  1 pk and 20 pk.

## Reason for recall

Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.

## Distribution

Worldwide - US Nationwide distribution including in the states of AK, AL, AP, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WI, WV, WY and the countries of AE, AT,  AU, BR, CA	, CH, CZ, DE, DZ, EE, ES, FI, FR, GB, GR, HR, HU, IE, IL, IT, JP, KW, KY, LT, MA, MY, NL, NO, NZ, PL, PR, PT, RO, SE, SG, SK, TR.

## Key facts

- **Recall number:** Z-2444-2025
- **Recalling firm:** Orascoptic Surgical Acuity
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-03
- **Report date:** 2025-09-03

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2444-2025

## Citation

> AI Analytics. FDA recall Z-2444-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2444-2025. Source: US FDA. Licensed CC0.

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