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Recall for proCART trephines, Aesculap

2008.09.01

Product group Medical instruments for use in humans
Reference 02600/07

Recall of the products proCART trephines (Art. Numbers see annex, all lots) from Aesculap AG. The firm has initiated the recall, because the firm received reports about torsion fractures of the instruments after overload conditions.

Recall for proCART trephines, Aesculap , Download_VeroeffentlichtAm_EN PDF, 104KB, File does not meet accessibility standards

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