Maquet Cardiovascular Us Sales, Llc: Medical Device Recall in 2013 - (Recall #: Z-1572-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solutions into the systemic circulation during pediatric extracorporeal circulation procedures.

Product Classification:

Class II

Date Initiated: May 14, 2013

Date Posted: July 3, 2013

Recall Number: Z-1572-2013

Event ID: 65417

Reason for Recall:

The specified part numbers and lot numbers of Maquet Pediatric Arterial Cannula Packs may contain an incorrectly sized connector.

Status: Terminated

Product Quantity: 100 units (60 Domestic; 40 International)

Code Information:

Catalogue Number:Part Number: Lot Number are as follows: (1) 161410 (10 FR.):701022682:92056588 (2) 163610 (10 Fr):70102597:92059789 (3) 163608 (8 Fr.):70102.2681:92065640 (4) 163606 (6 Fr.):70102.2680:92063566

Distribution Pattern:

Worldwide Distribution - US Distribution including the states of Delaware, Illinois, Minnesota , New York., Ohio and Pennsylvania and the countries of Germany, Turkey and France.

Voluntary or Mandated:

Voluntary: Firm initiated