MICROspecialties recalls Synerget: I Pack Injection Kit with Wire Speculum-Tray (Model 18069W) due to potential infection from improper sterilization.
Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
MICROspecialties is recalling their Synergetics I Pack Injection Kit with Wire Speculum-Tray (Model 18069W) because it may not have been properly sterilized, risking post-operative infections. This affects medical professionals and patients who use the kit for eye injections.
The kit may not have been exposed to the correct sterilization cycle, which could lead to infections at the injection site or after surgery. This happens because the sterilization process is critical for preventing contamination.
Medical professionals and patients who use this kit for eye injections are affected. The risk is low as the hazard is related to improper sterilization rather than immediate harm.
Check for the model number 18069W or catalog number 18069W on the kit. The lot number P62764970R and unique device identifier 10841305101132 are also associated with this recall.
Look for the model number 18069W or catalog number 18069W on the kit.
The kit may not have been properly sterilized, which could lead to post-operative or injection site infections.
The recall record does not specify a remedy, so check with the manufacturer for guidance.
The recall states a potential infection risk, but not a risk of serious injury, so the danger level is low.
We’ve drafted a message you can send MICROspecialties to request your refund or repair — edit it as you like.
Subject: Recall Z-2336-2024 — MICROspecialties MICROspecialties Hello, I own a MICROspecialties that is covered by recall Z-2336-2024 from MICROspecialties. 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.
