Alto Development Corp recalls surgical punches due to potential packaging damage during shipping, risking loss of sterility. Affected units include specific model numbers with varying quantities.
Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility.
Alto Development Corp is recalling surgical punches that may have been damaged during shipping, risking loss of sterility. This could lead to infections if the devices are used without proper sterilization.
The packaging may have been damaged during transportation, which could compromise the sterility of the surgical punches. If the device is not sterile, it could lead to infections during surgery.
Trained surgeons who use these surgical punches for creating circular cuts during procedures are most at risk. The recall affects specific model numbers sold in limited quantities.
Check for model numbers 080-271, 080-351, 080-401, 080-403, 080-451, or 080-481, 080-501 on the punch shelf box. These models were sold in specific quantities between the listed numbers.
Look for model numbers 080-271, 080-351, 080-401, 080-403, 080-451, 080-481, or 080-501 on the punch shelf box.
The surgical punches may have been damaged during transportation, risking loss of sterility.
Model numbers 080-271, 080-351, 080-401, 080-403, 080-451, 080-481, and 080-501.
9108 units of model 080-271, 41712 units of model 080-351, 219954 units of model 080-401, 1368 units of model 080-403, 83190 units of model 080-451, 32556 units of model 080-481, and 23598 units of model 080-501.
We’ve drafted a message you can send Alto Development Corp to request your refund or repair — edit it as you like.
Subject: Recall Z-0813-2018 — Alto Development Corp Alto Development Corp Hello, I own a Alto Development Corp that is covered by recall Z-0813-2018 from Alto Development Corp. 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.
