Visitec LASIK IRR Cannula (Catalog #585278) recalled due to temperature excursions between June 1 and August 30, 2021, potentially affecting product effectiveness.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Visitec LASIK IRR Cannula (Catalog #585278) was recalled because it may have been exposed to higher temperatures between June 1 and August 30, 2021, which could impact its effectiveness. This recall affects medical facilities that received the product during that period.
The cannula may have been exposed to higher temperatures during shipping or storage between June 1 and August 30, 2021. This temperature exposure could potentially reduce the product's effectiveness for LASIK procedures.
Medical facilities that received the Visitec LASIK IRR Cannula (Catalog #585278) between June 1 and August 30, 2021. Patients using this cannula for LASIK procedures may be at risk if the product was exposed to higher temperatures during storage.
Check if your Visitec LASIK IRR Cannula (Catalog #585278) was received by your medical facility between June 1 and August 30, 2021. The product has a catalog number of 585278 and GTIN 30886158002995.
Verify if your Visitec LASIK IRR Cannula (Catalog #585278) was received between June 1 and August 30, 2021.
The product was recalled because it may have been exposed to higher temperatures between June 1 and August 30, 2021, which could impact its effectiveness for LASIK procedures.
Check if your Visitec LASIK IRR Cannula (Catalog #585278) was received between June 1 and August 30, 2021. If so, contact your medical facility for further instructions.
The recall indicates a potential impact on product effectiveness, but no specific injury risk is mentioned in the official notice.
We’ve drafted a message you can send Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-1626-2022 — Visitec Visitec Hello, I own a Visitec that is covered by recall Z-1626-2022 from Visitec. 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.
