AbbVie Inc.
2 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (2)
Registered facilities (5)
- AbbVie Deutschland GmbH & Co.KG FEI 3002807401 · DE
- AbbVie Ireland NL B.V. Ballytivnan FEI 3012441529 · IE
- AbbVie US LLC FEI 3009751352 · IL
- AbbVie Inc FEI 3010757606 · IL
- AbbVie Inc. FEI 3004217756 · AZ
Recalls & enforcement
- Class IITerminated2017-04-27
- Class IITerminated2016-11-22AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “AbbVie Inc. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10046068-abbvie-inc/
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