Olympus recalls INJECTOR FORCEMAX UP 2.1G 6MM needles with inadequate package seals that may cause infections. Affected models include NM-400L-0621 and specific batch codes. Stop using if you have these items.
Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.
Olympus is recalling certain endoscopic injection needles because some sterile packages have poor seals, which could lead to infections if used improperly. This affects patients who use these needles for digestive tract treatments. The recall is for specific model numbers and batch codes.
The sterile packages may have inadequate seals due to partial heat sealing. If the package isn't properly sealed, the needles could become non-sterile, increasing the risk of infection during medical procedures.
Patients using endoscopic injection needles for digestive tract treatments. Those with the specific model numbers and batch codes listed are most at risk.
Check for model number NM-400L-0621 and batch codes 01K, 02K, 03K, 07K, 08K, 09K, 0XK, 98K, 99K, 9XK, 9YK, 9ZK, 05V, 06V, 07V, 08V, 09V, 0XV on the packaging.
Inspect the sterile package for signs of inadequate sealing, such as gaps or improper heat sealing.
The recall states that some packages have inadequate seals, which could lead to infections. If you have the affected model numbers, stop using them immediately.
The recall does not specify a remedy, so you should check the package seal and contact Olympus if you have concerns.
Yes, the affected batch codes include 01K, 02K, 03K, 07K, 08K, 09K, 0XK, 98K, 99K, 9XK, 9YK, 9ZK, 05V, 06V, 07V, 08V, 09V, 0XV.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0998-2021 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0998-2021 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.
