Abbott Gmbh & Co. KG recalls

Abbott Gmbh & Co. KG has 19 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 5 Aug 2020. 4 are still ongoing. The most frequent reason is device malfunction.

Total recalls19since 2018
Last 12 months0reported
Class I00% of total
Ongoing4latest 5 Aug 2020

Recalls per month, last 24 months

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Severity split

Class I 0 0%Class II 19 100%Class III 0 0%

Why abbott gmbh & co. kg is recalled

By year

Ongoing abbott gmbh & co. kg recalls

4 active

All abbott gmbh & co. kg recalls, newest first

19 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIAlinity ci series System Control Module (SCM) recalledAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIAlinity C, Processing Module recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGPotency & Assay25 states
DeviceCLASS IIArchitect iGentamicin Reagent Kit recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGPotency & AssayNationwide
DeviceCLASS IIArchitect Havab G Reagent Kit recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGHepatitis ANationwide
DeviceCLASS IILN 3R70 recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIAccessory kit, Alinity c containing Alinity ci Level Sensor recalledAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIAlinity ci Level Sensor, Bulk Solution recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIAlinity c Carbon Dioxide Reagent Kit, Produced recalledAbbott GmBH & Co. KGOtherNationwide
DeviceCLASS IIAccessory kit, Alinity i containing Alinity ci Level Sensor recalledAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIArchitect Havab-g Calibrator recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGOther22 states
DeviceCLASS IIAlinity ci -series System Control¿Module recalledAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIThe Alinity ci-series System Control Modules recalledAbbott Gmbh & Co. KGPotency & AssayNationwide
DeviceCLASS IIAlinity c Cuvette Segments, List Number 04S47 recalledAbbott Gmbh & Co. KGOtherNationwide
DeviceCLASS IIAlinity i Processing Module, 03R65 01, with the below components recalledAbbott Gmbh & Co. KGTemperature AbuseNationwide
DeviceCLASS IIAbbott Alinity ci-series System Control Module recalledAbbott Gmbh & Co. KGDevice Malfunction19 states
DeviceCLASS IIAbbott Alinity i Processing Module LN 03R65 recalledAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIAbbott Alinity c Processing Module LN 03R67 recalledAbbott Gmbh & Co. KGDevice MalfunctionNationwide
DeviceCLASS IIAlinity i Processing Module, (a) recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGPotency & AssayN/A
DeviceCLASS IIArchitect Dhea-s Reagent recalled by Abbott Gmbh & Co. KGAbbott Gmbh & Co. KGPotency & Assay31 states

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.