Medical Device Recall: Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS);
Maquet Cardiopulmonary Gmbh · July 31, 2026
Reason for Recall
The packaging may not consistently maintain sterile barrier integrity.
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belarus, Belgium, Brazil, Canada, China, Colombia, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, India, Ireland, Italy, Japan, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom;
States Affected
NATIONWIDE
Quantity Affected
185617 units (5926 US, 179691 OUS)
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3145-2026
Status: ongoing
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