Recall for Interpulse Systems, Stryker
2010.12.02
Product group Surgical equipment/ Anaesthesia
Reference 03771/10
Stryker GmbH & Co. KG has issued a recall of Interpulse Systems 0210100000/E / 0210110000/E, 0210114000/E. There is potential for a bread in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection.
Recall for Interpulse Systems, Stryker , Download_VeroeffentlichtAm_EN