Olympus recalls Paparrela-Type Vent Tubes due to missing expiration date on inner packaging. The outer box shows expiration date February 12, 2033. Consumers should check packaging for missing expiration date.
The expiration date is missing from the primary (inner) packaging. The secondary (outer) box label correctly states the expiration date of February 12, 2033, for this lot
Olympus is recalling Paparrela-Type Vent Tubes because the inner packaging lacks an expiration date. This could lead to using expired tubes, which might not be sterile or effective for ear ventilation after ear infections.
The inner packaging does not show an expiration date. This means users might use tubes that have expired, potentially compromising sterility or effectiveness for ear ventilation after infections.
People who own or use Olympus Paparrela-Type Vent Tubes for ear infections. Those most at risk are individuals who rely on these tubes for middle ear ventilation after otitis media.
Check the inner packaging for an expiration date. The outer box label shows expiration date February 12, 2033 for lot number SM280573. The product is a 1.02mm silicone vent tube for middle ear ventilation after ear infections.
Look for an expiration date on the inner packaging of the vent tube. If missing, it is part of the recall.
The inner packaging lacks an expiration date, which could lead to using expired tubes that might not be sterile or effective for ear ventilation after infections.
The outer box label shows expiration date February 12, 2033 for lot number SM280573.
The recall record does not specify a return or remedy, so no action is required beyond checking the inner packaging for an expiration date.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1004-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1004-2024 from Olympus. 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.
