How many recalls does Maquet Cardiovascular, LLC have?

Recalert has 71 U.S. recalls on record for Maquet Cardiovascular, LLC, published between January 16, 2013 and July 22, 2026.

Which agencies have handled Maquet Cardiovascular, LLC recalls?

Maquet Cardiovascular, LLC appears as the recalling firm in recalls from: FDA (71).

Maquet Cardiovascular, LLC: 71 recalls on record

Recalls filed with 1 agency: FDA (71).

First recall on record: January 16, 2013. Most recent: July 22, 2026.

Risk classification: Class I: 3 · Class II: 68

Most recent recalls

Date	Agency	Product	Recall number
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 24202 ADULT ECC Material:701054295Z-1532-2019	Z-1532-2019
June 5, 2019	FDA	Maquet Getinge BO-TOP 48400 OR PACK Material: 701064327R01Z-1659-2019	Z-1659-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-T 4917 Mercy Medical Versa-Pack Material: 709000368Z-1612-2019	Z-1612-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 21502# Med City Childr Material: 701050060Z-1506-2019	Z-1506-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 5502 ECC Pack Material:701051791R01Z-1640-2019	Z-1640-2019
June 5, 2019	FDA	Maquet Getinge-BO-TOP 15200 OR PACK HMO & RF Material:701050647R01Z-1638-2019	Z-1638-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 5208 ECC SET CARDIAC Material: 701067350Z-1585-2019	Z-1585-2019
June 5, 2019	FDA	Maquet Getinge- BEQ-TOP 37200 E-Circuit Bioline Heparin Material: 701055388R01Z-1652-2019	Z-1652-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 37500 ECC QUADROX ID Material: 701055601Z-1540-2019	Z-1540-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 8075 S-Quadrox iD Plus Pack wRF3 Material: 709000460Z-1623-2019	Z-1623-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 3700 Tubing Pack Material: 701049510Z-1504-2019	Z-1504-2019
June 5, 2019	FDA	Maquet Getinge-BO-T 6600 TUBING PACK Material:701052324Z-1520-2019	Z-1520-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-T 8805 ECC PACK Material: 701053361Z-1525-2019	Z-1525-2019
June 5, 2019	FDA	Maquet Getinge-BEQ-TOP 44701 PEDIATRIC ECC Material: 701064825Z-1561-2019	Z-1561-2019
March 13, 2019	FDA	AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is inten…Z-0983-2019	Z-0983-2019
March 22, 2017	FDA	VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage: The VASO…Z-1456-2017	Z-1456-2017
November 5, 2014	FDA	Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump System OM-9000…Z-0132-2015	Z-0132-2015
December 18, 2013	FDA	Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular LLC 45 Barbour…Z-0466-2014	Z-0466-2014
October 9, 2013	FDA	Ultima OPCAB System, Sterile, Rx Only, Product Usage: Intended for use during perfor…Z-0001-2014	Z-0001-2014
April 24, 2013	FDA	MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version 3.3.0.0) Produ…Z-1149-2013	Z-1149-2013
January 16, 2013	FDA	CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate and d…Z-0662-2013	Z-0662-2013

Questions about this company

How many recalls does Maquet Cardiovascular, LLC have?: Recalert has 71 U.S. recalls on record for Maquet Cardiovascular, LLC, published between January 16, 2013 and July 22, 2026.
Which agencies have handled Maquet Cardiovascular, LLC recalls?: Maquet Cardiovascular, LLC appears as the recalling firm in recalls from: FDA (71).

Do you carry products from Maquet Cardiovascular, LLC? Check your whole catalog free against 80,000+ recalls.

Paste up to 100 UPCs or SKUs and see which ones match a CPSC, FDA, NHTSA or FSIS recall. No account needed.

Check my catalog free

Want it checked every night instead? Starter watches 500 SKUs for $29/month. See plans

Maquet Cardiovascular, LLC: 71 recalls on record

Most recent recalls

Questions about this company

Do you carry products from Maquet Cardiovascular, LLC? Check your whole catalog free against 80,000+ recalls.

Related companies