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 potency & assay.
Total recalls19since 2018
Last 12 months0reported
Class I00% of total
Ongoing4latest 5 Aug 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 19 100%Class III 0 0%
Why abbott gmbh & co. kg is recalled
Product types
By year
Ongoing abbott gmbh & co. kg recalls
4 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Architect iGentamicin Reagent Kit recalled by Abbott Gmbh & Co. KG | Abbott Gmbh & Co. KG | Potency & Assay | Nationwide |
| Device | CLASS II | Accessory kit, Alinity c containing Alinity ci Level Sensor recalled | Abbott Gmbh & Co. KG | Device Malfunction | Nationwide |
| Device | CLASS II | Alinity ci Level Sensor, Bulk Solution recalled by Abbott Gmbh & Co. KG | Abbott Gmbh & Co. KG | Device Malfunction | Nationwide |
| Device | CLASS II | Accessory kit, Alinity i containing Alinity ci Level Sensor recalled | Abbott Gmbh & Co. KG | Device Malfunction | Nationwide |
All abbott gmbh & co. kg recalls, newest first
19 totalAbout 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.