Orascoptic recalls 2023-2025 Superior Visualization Phantom Essential kits due to nickel in nose pads causing allergic reactions. Affected kits include nose pads, screws, and cleaning wipes. Contact for remedy.
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
Orascoptic is recalling its Superior Visualization Phantom Essential kits made from June 2023 to May 2025 because nose pads contain nickel that can cause allergic reactions. This affects users who may develop skin irritation or more severe reactions.
The nose pads in these kits contain nickel, a metal that can cause allergic reactions in sensitive individuals. This may lead to skin irritation, redness, or more severe reactions in people with nickel allergies. The risk is not immediate but depends on exposure.
Users of the Orascoptic Superior Visualization Phantom Essential kits made between June 2023 and May 2025 are most at risk, particularly those with nickel allergies. People who use these kits for medical procedures or training may be affected.
Check for kits with nose pads, screws, lens cleaning wipes, side shields, and head straps manufactured between June 6, 2023, and May 14, 2025. The product name is 'Orascoptic Superior Visualization Phantom Essential Kit'.
If you have skin irritation, redness, or other signs of an allergic reaction, stop using the kit immediately.
Orascoptic will provide a remedy for affected kits, but the recall record does not specify the exact remedy.
The recall covers all Orascoptic Superior Visualization Phantom Essential kits manufactured between June 6, 2023, and May 14, 2025.
The nose pads contain nickel, which can cause allergic reactions in sensitive individuals.
The recall does not specify an immediate stop-use requirement; however, if you have a nickel allergy, you should avoid using the kit.
We’ve drafted a message you can send Orascoptic to request your refund or repair — edit it as you like.
Subject: Recall Z-2443-2025 — Orascoptic Orascoptic Hello, I own a Orascoptic that is covered by recall Z-2443-2025 from Orascoptic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
