Olympus recalls SOLTIVE SuperPulsed Laser Fibers with mismatched model sizes between carton, pouch, and device. Affected lots may cause injury if used incorrectly. Return or stop using immediately.
Device model and size for affected lots of Laser Fibers may be mismatched between the product's carton, immediate pouch packaging, and/or the device.
Olympus is recalling SOLTIVE SuperPulsed Laser Fibers due to mismatched model sizes between the product's carton, pouch, and device. Using the wrong size fiber could cause injury if the laser fiber is not properly matched to the device.
The laser fibers may be mismatched between the carton label, pouch packaging, and the actual device. This mismatch could lead to using the wrong fiber size, which might cause injury during operation.
Users of SOLTIVE SuperPulsed Laser Fibers with the specific model numbers listed in the recall are affected. Those using the fibers for medical procedures or industrial applications are at higher risk.
Check the carton label for model numbers like TFL-FBX150BS, TFL-FBX200S, TFL-FBX200BS, TFL-FBX550S, or TFL-FBX365S. The recall includes specific lot numbers with corresponding model labels.
Look for model numbers on the carton, pouch, and device to ensure they match the listed model numbers in the recall.
If the model numbers on the carton, pouch, and device do not match, stop using the fiber immediately to avoid potential injury.
The affected model numbers include TFL-FBX150BS, TFL-FBX200S, TFL-FBX200BS, TFL-FBX550S, and TFL-FBX365S.
Check the carton label for model numbers listed in the recall and compare with the lot numbers provided.
The recall does not specify a return process, so contact Olympus directly for instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1296-2022 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1296-2022 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.
