Lack of pouch seal. Product is labelled as sterile.
TeDan Surgical Innovations
Lack of pouch seal. Product is labelled as sterile.
Lack of pouch seal. Product is labelled as sterile.
Lack of pouch seal. Product is labelled as sterile.
Lack of pouch seal. Product is labelled as sterile.
Lack of pouch seal. Product is labelled as sterile.
Lack of pouch seal. Product is labelled as sterile.
There was incorrect raw material used in the production of the identified lot.
The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product to non sterile conditions. This situation presents a risk of infection to patients.
The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product to non sterile conditions. This situation presents a risk of infection to patients.
The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product to non sterile conditions. This situation presents a risk of infection to patients.
The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product to non sterile conditions. This situation presents a risk of infection to patients.
This letter is to notify you that several of our sterile screw products are being voluntarily recalled. Product sterility may be compromised due to a mechanical failure of the protective packaging tube. Tube end plugs may dislodge creating the potential for the screw to come out of the protective tube and then the sharp end of the screw pierce the outer sterile barrier pouch.