Orascoptic Superior Visualization (Orascoptic) – Nickel Allergy Risk (2025)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Orascoptic Superior Visualization Custom loupes with Dragonfly frames
Brand
Orascoptic Surgical Acuity
Lot Codes / Batch Numbers
All Serial numbers manufactured between September 7, 2023 - May 14, 2025
Products Sold
All Serial numbers manufactured between September 7, 2023 - May 14, 2025
Orascoptic Surgical Acuity is recalling Orascoptic Superior Visualization Custom loupes with Dragonfly frames due to Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
Recommended Action
Per FDA guidance
On June 24, 2025, Orascoptic Superior Visualization issued a Urgent: Loupe Advisory Notice. On July 7, 2025 a revised letter was issued to remove cleaning instructions. On August 13, 2025, Orascoptic Superior Visualization issued an Urgent: Medical Device Recall expansion notification to include additional nose pad accessory kits and additional information on the reason for recall, the risk to patient and the steps that should be taken. Orascoptic asked consignees to take the following actions: 1. To confirm if your loupe is subject to this notice, please visit orascoptic.com website to search the serial number. " Dragonfly loupe: the serial number is printed on the inside of the right temple arm. " Phantom sport frame: the serial number is printed on the loupe case name badge plate. 2. If you have given your custom loupe to someone else, please forward a copy of this notice to that person. 3. To request a replacement nose pad that does not contain nickel, please visit orascoptic.com. 4. Visit Orascoptic.com for directions on how to replace the nose pad for your frame. Contact technical support if you need additional support at 800.369.3698. Please discard the old nose pad. 5. Acknowledge receipt of this notice and contacting Orascoptic.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026