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Bess pro GmbH recalls a batch of Aerstent TBY airway stents in France
Bess pro GmbH has carried out a lot recall of the Aerstent TBY tracheobronchial prosthesis. France's medicines safety agency ANSM was informed and registered the action under number R2632267. The notice is aimed at pharmacies for internal use and healthcare establishments. Affected users received a letter from the company, but the source does not describe the nature of the problem.
What does it mean?
A company is recalling a batch of a device used in patients' airways. People who use this product, or who handle it in healthcare settings, should pay attention to the company's letter.
Who is affected?
Patients using the Aerstent TBY, and pharmacies and healthcare establishments that hold this product in stock.