Getinge Us Sales recalls

Getinge Us Sales has 12 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 18 Dec 2019. 1 is still ongoing.

Total recalls12since 2018

Last 12 months0reported

Class I00% of total

Ongoing1latest 18 Dec 2019

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 11 92%Class III 1 8%

Why getinge us sales is recalled

Product types

By year

2019975%
2018325%

Ongoing getinge us sales recalls

1 active

Reported	Class	Recall	Company	Reason	Where
18 Dec 2019Device	CLASS II	Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric recalled	Getinge Us Sales	Sterility	Nationwide

All getinge us sales recalls, newest first

12 total

Reported	Class	Recall	Company	Reason	Where
18 Dec 2019Device	CLASS II	Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric recalled	Getinge Us Sales	Sterility	Nationwide
2 Oct 2019Device	CLASS II	The Hemashield Platinum Woven Double Velour Vascular Graft recalled	Getinge Us Sales	Other	NJ
11 Sep 2019Device	CLASS II	Getinge MCC Flow i Disposable CO2 absorber, used recalled	Getinge Us Sales	Other	Nationwide
31 Jul 2019Device	CLASS II	PulsioFlex Monitoring System recalled by Getinge Us Sales	Getinge Us Sales	Other	Nationwide
1 May 2019Device	CLASS III	Maquet Servo-I Ventilator System -EDI Catheter PHT Free recalled	Getinge Us Sales	Other	Nationwide
13 Mar 2019Device	CLASS II	Maquet XS Flat Screen Monitor Holder, SAT XS32 12 SPE, Configuration recalled	Getinge Us Sales	Other	AZ, TX
13 Mar 2019Device	CLASS II	Maquet XS Flat Screen Monitor Holder recalled by Getinge Us Sales	Getinge Us Sales	Other	AZ, TX
13 Mar 2019Device	CLASS II	Maquet XS Flat Screen Monitor Holder, PWD50+DF XS32 K3 SPE recalled	Getinge Us Sales	Other	AZ, TX
13 Mar 2019Device	CLASS II	Maquet XS Flat Screen Monitor Holder, XS32 SPE, Configuration recalled	Getinge Us Sales	Other	AZ, TX
30 May 2018Device	CLASS II	ALM XTEN Surgical Light intended to provide visible recalled	Getinge Us Sales	Device Malfunction	NJ

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.