Maquet Cardiovascular Us Sales, Llc: 23 recalls on record

Recalls filed with 1 agency: FDA (23).

First recall on record: July 18, 2012. Most recent: December 23, 2020.

Risk classification: Class I: 2 · Class II: 19 · Class III: 2

Most recent recalls

DateAgencyProduct
December 23, 2020FDAHLS Set Advanced, Model: BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Product Code/Part Number:…Z-0633-2021
December 23, 2020FDAHLS Set Advanced Model Name: BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code/Part Nu…Z-0632-2021
October 28, 2020FDAYuno Mobile Operating Table - Product Usage: Intended for support and position the patien…Z-0132-2021
September 23, 2020FDAMaquet/Getinge Rotaflow System Console US (115 V / 60 Hz) - Product Usage: Instructions f…Z-2957-2020
April 8, 2020FDAAvalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039Z-1603-2020
March 4, 2020FDAGetinge 46-Series Washer Disinfector Model # 46-4, Part Number:46-4-502 Product Usage: Us…Z-1390-2020
December 18, 2019FDAMaquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device …Z-0678-2020
July 3, 2019FDAMaquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model: VST66DFZ-1864-2019
September 14, 2016FDAThe Connecting Bracket (Fixture) Device (1002.65A0) is designed as a connecting element t…Z-2746-2016
April 20, 2016FDARotaflow Centrifugal Pump Custom tubing packs for the oxygenatorZ-1373-2016
July 29, 2015FDAMagnus Hybrid OR Table Column (1180.01B2) used in conjunction with Siemens Artis Zeego An…Z-2097-2015
December 31, 2014FDAMaquet Quadrox-ID Pediatric Diffusion Membrane Oxygenator with Bioline Coating; Part Numb…Z-0870-2015
November 19, 2014FDACardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide removal sy…Z-0211-2015
March 19, 2014FDAMAQUET PLEGIOX Cardioplegia Heat Exchanger The PLEGIOX Cardioplegia Heat Exchanger is …Z-1165-2014
February 5, 2014FDACompressor Mini To provide a supply of dry, filtered compressed air for a medical resp…Z-0848-2014
October 2, 2013FDATEGRIS system Four labels of the Tegris System include: Emergency button (1703.72)…Z-2275-2013
October 2, 2013FDAQUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000…Z-2262-2013
July 10, 2013FDAMAQUET Getinge Group Mobile Operating Table YUNO OTN GA 1433.01 EN 05. The YUNO OTN is…Z-1622-2013
July 3, 2013FDAMAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solution…Z-1572-2013
May 8, 2013FDAMaquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part…Z-1177-2013
February 27, 2013FDAMaquet ELS Cannula 15 FR. Used for extracorporeal membrane oxygenation (ECMO) for the tre…Z-0839-2013
November 7, 2012FDAQUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000…Z-0160-2013
July 18, 2012FDAFLOW-I Anesthesia System The system is intended for use in administrating anesthesia w…Z-1925-2012

Questions about this company

How many recalls does Maquet Cardiovascular Us Sales, Llc have?
Recalert has 23 U.S. recalls on record for Maquet Cardiovascular Us Sales, Llc, published between July 18, 2012 and December 23, 2020.
What was the most recent Maquet Cardiovascular Us Sales, Llc recall?
FDA recall Z-0633-2021, published December 23, 2020: HLS Set Advanced, Model: BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Product Code/Part Number: 70105.2794 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorpor…
Which agencies have handled Maquet Cardiovascular Us Sales, Llc recalls?
Maquet Cardiovascular Us Sales, Llc appears as the recalling firm in recalls from: FDA (23).

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