MICROspecialties recalls Syner: 18061 injection kits that may not have been properly sterilized, risking post-op infections. Affected units include specific model and lot numbers.
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 Drape (model 18061) because it may not have been properly sterilized, which could lead to post-operative or injection site infections. This recall affects medical professionals using the kit for eye injections.
The injection kit may not have been exposed to the correct sterilization cycle, which could lead to contamination. This contamination might cause infections at the surgical site or injection area after use.
Medical professionals who use this kit for ophthalmic injections are most at risk. The recall applies to specific model and lot numbers sold to healthcare providers.
Check for the model number 18061 on the kit. The lot number P63044983R is associated with this recall. The product was sold with a unique device identifier (UDI) 10841305101071.
Look for the model number 18061 and lot number P63044983R 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 or action steps beyond checking product details.
The recall states a risk of infection, but not serious injury or death. The danger level is low risk.
We’ve drafted a message you can send MICROspecialties to request your refund or repair — edit it as you like.
Subject: Recall Z-2334-2024 — MICROspecialties MICROspecialties Hello, I own a MICROspecialties that is covered by recall Z-2334-2024 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.
