MICROspecialties recalls Synerget: I Pack Injection Kit Custom-Tray (Model 18069) due to potential infection from improper sterilization. Affected units may cause post-op wound or injection site infections.
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 Synergetics I Pack Injection Kit Custom-Trays (Model 18069) because they might not have been properly sterilized, which could lead to infections after eye surgery or injections. This affects medical users who rely on these kits for ophthalmic procedures.
The kits may not have gone through the correct sterilization process, which can lead to infections at the injection site or after surgery. This happens because improper sterilization allows bacteria to survive in the kit.
Medical professionals using this injection kit for eye procedures are most at risk. Patients receiving ophthalmic injections with this kit could face infection.
Check for the model number 18069 on the Synergetics I Pack Injection Kit Custom-Tray. The product was sold with a lot number P62764965R and a unique device identifier 10841305101125.
Look for the model number 18069 and lot number P62764965R on the Synergetics I Pack Injection Kit Custom-Tray.
The recall states a potential for infection, but not a risk of serious injury like death or major harm. The hazard is limited to post-operative wound or injection site infections.
Check for model number 18069 and lot number P62764965R on the Synergetics I Pack Injection Kit Custom-Tray.
The recall does not specify a remedy, so you should check with MICROspecialties directly for guidance.
We’ve drafted a message you can send MICROspecialties to request your refund or repair — edit it as you like.
Subject: Recall Z-2335-2024 — MICROspecialties MICROspecialties Hello, I own a MICROspecialties that is covered by recall Z-2335-2024 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.
